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

GILLUM'S WHEELCHAIR WIDTH REDUCING ATTACHMENT

K Number: K884052 · Decision Oct 26, 1988
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
63
Applicant Total
1
Review Days
30

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
GILLUM'S WHEELCHAIR WIDTH REDUCING ATTACHMENT
K Number
K884052
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3920
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Professional Service Unltd.
Date Received
September 26, 1988
Decision Date
October 26, 1988
Product Code
KNN
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
KNN Components, Wheelchair

Similar 510(k) Clearances

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

View all