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

STRYKER POWERED WHEELED STRETCHER

K Number: K022309 · Decision Nov 8, 2002
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
11
Applicant Total
124
Review Days
115

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Basic Information

Device Name
STRYKER POWERED WHEELED STRETCHER
K Number
K022309
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3690
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Corp.
Date Received
July 16, 2002
Decision Date
November 8, 2002
Product Code
INK
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
INK Stretcher, Wheeled, Powered

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K150449 LITe Plate System
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K133671 ICONIX ALL SUTURE ANCHORS
K122113 MEMORY METAL STAPLES, EASYCLIP
K122284 HOFFMANN 3
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