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

ELECTRIC SEAT LIFT CHAIR

K Number: K961663 · Decision May 29, 1996
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
52
Applicant Total
2
Review Days
56

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Basic Information

Device Name
ELECTRIC SEAT LIFT CHAIR
K Number
K961663
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3110
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ken Kemmerer
Date Received
April 3, 1996
Decision Date
May 29, 1996
Product Code
INO
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
INO Chair, Positioning, Electric

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K Number Device Name
K935351 A.C. POWER PATIENT LIFT