510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K053572Substantially Equivalent

C. Diff Quik Chek

Techlab, Inc., Blacksburg VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K053572 is the FDA 510(k) clearance record for C. DIFF QUIK CHEK, a class I device, cleared for Techlab, Inc. on under FDA product code MCB (Antigen, C. Difficile). FDA records list 36 510(k) clearances for Techlab, Inc., from to . As of , FDA records show no recalls naming K053572.

Clearance record

Decision date
Received
(125 days to decision)
Product code
MCB Antigen, C. Difficile
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Applicant
Techlab, Inc. 2001 Kraft Dr., Blacksburg VA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MCB

Trailing 12 months

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

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