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2. LGA 1700 - Wikipedia

   en.wikipedia.org/wiki/LGA_1700

   LGA 1700 (Socket V) is a zero insertion force flip-chip land grid array (LGA) socket, compatible with Intel desktop processors Alder Lake and Raptor Lake, which was first released in November 2021. LGA 1700 is designed as a replacement for LGA 1200 (known as Socket H5 ) and it has 1700 protruding pins to make contact with the pads on the processor.

3. List of Intel chipsets - Wikipedia

   en.wikipedia.org/wiki/List_of_Intel_chipsets

   Intel i945GC northbridge with Pentium Dual-Core microprocessor. This article provides a list of motherboard chipsets made by Intel, divided into three main categories: those that use the PCI bus for interconnection (the 4xx series), those that connect using specialized "hub links" (the 8xx series), and those that connect using PCI Express (the 9xx series).

4. Alder Lake - Wikipedia

   en.wikipedia.org/wiki/Alder_Lake

   LGA 1700 socket for desktop processors. ... 150 W 241 W $739 12900K: 3.2 2.4 5.1 3.9 ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...

5. Land grid array - Wikipedia

   en.wikipedia.org/wiki/Land_grid_array

   LGA 1700 socket on a motherboard.. The land grid array (LGA) is a type of surface-mount packaging for integrated circuits (ICs) that is notable for having the pins on the socket (when a socket is used) — as opposed to pins on the integrated circuit, known as a pin grid array (PGA). [1]

6. Raptor Lake - Wikipedia

   en.wikipedia.org/wiki/Raptor_Lake

   [6] [7] Raptor Lake features up to 24 cores (8 performance cores plus 16 efficiency cores) and 32 threads and is socket compatible with Alder Lake systems (LGA 1700, BGA 1744, BGA 1964). [8] [9] [10] Like earlier generations, Raptor Lake processors also need accompanying chipsets. Raptor Lake CPUs have suffered issues with permanent damage from ...

7. US FDA proposes standardized testing to detect asbestos in ...

   www.aol.com/us-fda-proposes-standardized-testing...

   If the manufacturer fails to comply with testing and record-keeping requirements, the proposed rule allows the FDA to declare that product as adulterated under the Federal Food, Drug, and Cosmetic ...