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

MICROAIR PUP

K Number: K925694 · Decision Mar 24, 1993
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
56
Applicant Total
1
Review Days
132

Basic Information

Device Name
MICROAIR PUP
K Number
K925694
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5170
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
GSI MEDICAL SYSTEMS
Date Received
November 12, 1992
Decision Date
March 24, 1993
Product Code
IOQ
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IOQ Bed, Flotation Therapy, Powered

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