FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GENTAMICIN DISK (120MCG)

K Number: K961818 · Decision Jul 10, 1996
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
327
Applicant Total
10
Review Days
61

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Basic Information

Device Name
GENTAMICIN DISK (120MCG)
K Number
K961818
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.1620
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Remel, L.P.
Date Received
May 10, 1996
Decision Date
July 10, 1996
Product Code
JTN
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
JTN Susceptibility Test Discs, Antimicrobial

Similar 510(k) Clearances

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

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Other Clearances by Remel, L.P.

K Number Device Name
K972359 REMEL BILE ESCULIN AZIDE AGAR W/6 MCG/ML VANCOMYCIN
K964315 REMEL STAPH LATEX KIT
K964421 REMEL MEROPENEM 10UG SUSCEPTIBILITY DISK
K961046 10B ARGININE BROTH
K955143 RPR LIQUID CONTROLS
K955136 RPR CARD TEST KIT
K961819 STREPTOMYCIN DISK (300MCG)
K960313 MUELLER HINTON AGAR WITH 2% NACI
K954986 GC BASE W/ 1% GCHI