510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K894712Substantially Equivalent

Accuprobe Campylobacter Culture Confirmation

Hologic, Inc., San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K894712 is the FDA 510(k) clearance record for ACCUPROBE CAMPYLOBACTER CULTURE CONFIRMATION, a class I device, cleared for Gen-Probe, Inc. on under FDA product code LQO (Dna-Reagents, Campylobacter Spp.). FDA records list 189 510(k) clearances for Hologic, Inc., from to . As of , FDA records show no recalls naming K894712.

Clearance record

Decision date
Received
(111 days to decision)
Product code
LQO Dna-Reagents, Campylobacter Spp.
Regulation
21 CFR 866.3110
Device class
Class I
Review panel
Microbiology
Applicant
Gen-Probe, Inc. 9880 Campus Pt. Dr., San Diego CA
Third party review
No

Clearances, product code LQO

Trailing 12 months

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

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