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

STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER

K Number: K940130 · Decision Mar 10, 1994
Classifications
1
FEI Numbers
124
Registration Numbers
124
Same Product Code
38
Applicant Total
124
Review Days
66

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Basic Information

Device Name
STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER
K Number
K940130
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6900
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Stryker Corp.
Date Received
January 3, 1994
Decision Date
March 10, 1994
Product Code
FPP
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
FPP Stretcher, Hand-Carried

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K122113 MEMORY METAL STAPLES, EASYCLIP
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