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

CAREMOR CLINER

K Number: K941569 · Decision Apr 26, 1994
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
34
Applicant Total
3
Review Days
26

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Basic Information

Device Name
CAREMOR CLINER
K Number
K941569
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3100
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Winco, Inc.
Date Received
March 31, 1994
Decision Date
April 26, 1994
Product Code
INM
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
INM Chair, With Casters

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K Number Device Name
K080533 WINCO MODEL POWER SERIES LIFT CHAIR
K933000 RECLINING GERI CHAIRS W/CASTERS & LAP TRAY