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

PORTABLE AUTOCLAVES

K Number: K830931 · Decision Jul 27, 1983
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
179
Applicant Total
1
Review Days
126

Basic Information

Device Name
PORTABLE AUTOCLAVES
K Number
K830931
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6880
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
ARNOLD & SONS
Date Received
March 23, 1983
Decision Date
July 27, 1983
Product Code
FLE
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
FLE Sterilizer, Steam

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