510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K902213Substantially Equivalent

Accuprobe Staphylococcus Aureus Culture Confirma.

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

K902213 is the FDA 510(k) clearance record for ACCUPROBE STAPHYLOCOCCUS AUREUS CULTURE CONFIRMA., a class I device, cleared for Gen-Probe, Inc. on under FDA product code MCS (Dna-Probe, Staphylococcus Aureus). FDA records list 189 510(k) clearances for Hologic, Inc., from to . As of , FDA records show no recalls naming K902213.

Clearance record

Decision date
Received
(82 days to decision)
Product code
MCS Dna-Probe, Staphylococcus Aureus
Regulation
21 CFR 866.3700
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 MCS

Trailing 12 months

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

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