510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K931241Substantially Equivalent

Fast'n'flammatory Kit

Techlab, Inc., Blacksburg VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K931241 is the FDA 510(k) clearance record for FAST'N'FLAMMATORY KIT, a class I device, cleared for Techlab, Inc. on under FDA product code GIA (Test, Leukocyte Peroxidase). FDA records list 36 510(k) clearances for Techlab, Inc., from to . As of , FDA records show no recalls naming K931241.

Clearance record

Decision date
Received
(329 days to decision)
Product code
GIA Test, Leukocyte Peroxidase
Regulation
21 CFR 864.7675
Device class
Class I
Review panel
Hematology
Applicant
Techlab, Inc. Vpi Research Park, Blacksburg VA
510(k) summary
Summary
Third party review
No

Clearances, product code GIA

Trailing 12 months

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

FDA records show no clearances under product code GIA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GIA, 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