510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K800925Substantially Equivalent

Verify S Prod. #34141

General Diagnostics, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K800925 is the FDA 510(k) clearance record for VERIFY S PROD. #34141, a class II device, cleared for General Diagnostics on under FDA product code GGW (Test, Time, Partial Thromboplastin). FDA records list 39 510(k) clearances for General Diagnostics, from to . As of , FDA records show no recalls naming K800925.

Clearance record

Decision date
Received
(91 days to decision)
Product code
GGW Test, Time, Partial Thromboplastin
Regulation
21 CFR 864.7925
Device class
Class II
Review panel
Hematology
Applicant
General Diagnostics 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GGW

Trailing 12 months
1 clearance under product code GGW in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GGW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260