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

STRYKER OPERATING ROOM TABLE

K Number: K940068 · Decision May 5, 1994
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
34
Applicant Total
14
Review Days
119

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Basic Information

Device Name
STRYKER OPERATING ROOM TABLE
K Number
K940068
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4960
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Stryker Medical
Date Received
January 6, 1994
Decision Date
May 5, 1994
Product Code
FQO
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FQO Table, Operating-Room, Ac-Powered

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