FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

RAPID IDENTIFI-METHOD NEISSERIA KIT

K Number: K830968 · Decision Jun 16, 1983
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
243
Applicant Total
45
Review Days
80

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Basic Information

Device Name
RAPID IDENTIFI-METHOD NEISSERIA KIT
K Number
K830968
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Austin Biological Laboratories
Date Received
March 28, 1983
Decision Date
June 16, 1983
Product Code
JTO
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JTO Discs, Strips And Reagents, Microorganism Differentiation

Similar 510(k) Clearances

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Other Clearances by Austin Biological Laboratories

K Number Device Name
K880511 XACT NEISSERIA
K874727 PRECEPT(TM) CIPROFLOXACIN
K870769 AUSTIN NONFERMENTER KIT
K864069 PRECEPT (TM) TICARCILLIN/CLAVULANIC ACID
K862560 PRECEPT CEFTIZOXIME
K862446 PRECEPT CEFTAZIDIME
K860195 PRECEPT TRIMETHOPRIM/SULFAMETHOXAZOLE
K860194 AUSTIN ENTERIC SYSTEM
K854577 PRECEPT AMOXICILLIN/CLAVVLANIC ACID (AUGMENTIN)
K853772 PRECEPT METHICILLIN
Search all 45 clearances from Austin Biological Laboratories →