Atlas FDA

ANAEROBE KIT

FDA 510(k) clearance K850052 · decided 1985-03-05

Clearance details

K-number
K850052
Device name
ANAEROBE KIT
Applicant
Austin Biological Laboratories
Decision
Substantially Equivalent
Date received
1985-01-08
Decision date
1985-03-05
Days to decision
56 days
Clearance type
Traditional
Product code
JSP
Device class
1
Regulation number
866.2660
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Austin, TX, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
LYFO(TM) DIFFERENTIAL DISK (K945488)Microbiologics, Inc.1995-05-11
LYFO(TM) DIFFERENTIAL DISK (K945489)Microbiologics, Inc.1995-05-11
LYFO(TM) DIFFERENTIAL DISK (K945487)Microbiologics, Inc.1995-05-11
BBLCRYSTAL ANAEROBE ID SYSTEM (K944528)Becton Dickinson Microbiology Systems1995-03-07
VITEK ANAEROBE IDENTIFICATION CARD, MODIFICATION (K910666)Vitek Systems, Inc.1991-04-03
VITEK ANAEROBE IDENTIFICATION CARD (K900996)Vitek Systems, Inc.1990-05-11
B. FRAGTEX (K881380)American Biomedical Products, Inc.1988-10-06
IDS RAPID ANA SYSTEM (K882960)Innovative Diagnostic Systems, Inc.1988-08-12
DIAGNOSTIC REAGENT PET-RPLA (K855235)Oxoid U.S.A., Inc.1986-11-04
ANAEROBE RAPID CHROMOGENIC ID PANEL (K862332)American Micro Scan1986-08-27
AMS ANA CARD (K843686)Vitek Systems, Inc.1984-12-12
API ANAIDENT (K831032)Analytical Products, Inc.1983-05-05

Recalls involving this device

No recalls on record reference this clearance.