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

KLORMAN

K Number: K923693 · Decision Jan 23, 1996
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
72
Applicant Total
14
Review Days
1279

Basic Information

Device Name
KLORMAN
K Number
K923693
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6890
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
MATRIX MEDICA, INC.
Date Received
July 23, 1992
Decision Date
January 23, 1996
Product Code
LRJ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
LRJ Disinfectant, Medical Devices

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