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

POWERMATIC EXAMINATION TABLE

K Number: K933577 · Decision Sep 30, 1993
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
101
Applicant Total
30
Review Days
70

Basic Information

Device Name
POWERMATIC EXAMINATION TABLE
K Number
K933577
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3760
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
MEDICAL DEVICE INSPECTION CO., INC.
Date Received
July 22, 1993
Decision Date
September 30, 1993
Product Code
INQ
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
INQ Table, Powered

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