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

GONOCHEK PANEL

K Number: K830756 · Decision Aug 12, 1983
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
243
Applicant Total
13
Review Days
155

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
GONOCHEK PANEL
K Number
K830756
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
E-Y Laboratories, Inc.
Date Received
March 10, 1983
Decision Date
August 12, 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

Other 510(k) clearances with the same product code (JTO), ordered by most recent decision date.

View all

Other Clearances by E-Y Laboratories, Inc.

K Number Device Name
K934130 SWABZYME OXIDASE
K940162 GONOCHEK II REAGENT TUBES
K940161 B-LACTAMASE REAGENT TUBES
K934125 GONOCHEK-II, MODIFICATION
K940124 EY-20 REAGENT TUBES
K940020 STREP-A-CHEK(TM) REAGENT STRIPS
K934129 STREP-A-CHEK
K844276 E-COLI-CHEK TUBE
K842600 STREP-A-CHEK
K840810 SWABZYME-OXIDASE
Search all 13 clearances from E-Y Laboratories, Inc. →