510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K896802Substantially Equivalent

Magnet Pad

Westmark, Sterile Packing Systems, Inc. (Sps), Grand Rapids MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K896802 is the FDA 510(k) clearance record for MAGNET PAD, a class I device, cleared for Westmark, Sterile Packing Systems, Inc. (Sps) on under FDA product code LXG (Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use). FDA records list 28 510(k) clearances for Westmark, Sterile Packing Systems, Inc. (Sps), from to . As of , FDA records show no recalls naming K896802.

Clearance record

Decision date
Received
(26 days to decision)
Product code
LXG Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use
Regulation
21 CFR 862.2050
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Westmark, Sterile Packing Systems, Inc. (Sps) 1253 Ramona St. SE, Grand Rapids MI
Third party review
No

Clearances, product code LXG

Trailing 12 months

FDA records hold no clearances under product code LXG in the trailing twelve months.

FDA records show no clearances under product code LXG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LXG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260