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

PORTABLE LIFT SEAT

K Number: K923804 · Decision Feb 12, 1993
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
52
Applicant Total
1
Review Days
198

Basic Information

Device Name
PORTABLE LIFT SEAT
K Number
K923804
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3110
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
FRANK H. SPECKHART, P.E.
Date Received
July 29, 1992
Decision Date
February 12, 1993
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (INO), ordered by most recent decision date.

View all