510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K910304Substantially Equivalent

Rapid Coryne Syst/identif of Coryneform Bacteria

Vitek Systems, Inc., Hazelwood MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K910304 is the FDA 510(k) clearance record for RAPID CORYNE SYST/IDENTIF OF CORYNEFORM BACTERIA, a class I device, cleared for Vitek Systems, Inc. on under FDA product code LQL (Gram Positive Identification Panel). FDA records list 39 510(k) clearances for Vitek Systems, Inc., from to . As of , FDA records show no recalls naming K910304.

Clearance record

Decision date
Received
(183 days to decision)
Product code
LQL Gram Positive Identification Panel
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Applicant
Vitek Systems, Inc. 595 Anglum Dr., Hazelwood MI
Third party review
No

Clearances, product code LQL

Trailing 12 months

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

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