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

REMEL CEFPODOXIME 10 MCG SUSCEPTIBILITY DISK

K Number: K931289 · Decision Jun 2, 1993
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
322
Applicant Total
137
Review Days
82

Basic Information

Device Name
REMEL CEFPODOXIME 10 MCG SUSCEPTIBILITY DISK
K Number
K931289
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.1620
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
REMEL CO.
Date Received
March 12, 1993
Decision Date
June 2, 1993
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.

View all

Other Clearances by REMEL CO.

K Number Device Name
K013711 BACTI-SWAB DRY
K965149 A.C.T. I
K965151 A.C.T. III
K965152 A.C.T. II
K965150 A.C.T. IV
K960090 CALCOFLUOR WHITE STAIN KIT
K960095 BACTIDROP CALCOFLUOR WHITE
K955669 REMEL CEFEPIME 30 UG SUSCEPTIBILITY DISK
K941443 SYNERGY QUAD
K941444 BHI AGAR WITH VANCOMYCIN
Search all 137 clearances from REMEL CO. →