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

STRYKER 5000

K Number: K935949 · Decision Jun 17, 1994
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
101
Applicant Total
14
Review Days
186

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Basic Information

Device Name
STRYKER 5000
K Number
K935949
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5550
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Stryker Medical
Date Received
December 13, 1993
Decision Date
June 17, 1994
Product Code
FNM
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
FNM Mattress, Air Flotation, Alternating Pressure

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K946149 STRYKER AGILITY INTENSIVE CARE BED
K943864 STRYKER 8000 SURGERY STRETCHER
K941738 STRYKER 5050 STRECHAIR
K940068 STRYKER OPERATING ROOM TABLE
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