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

GUS TRAC C-303

K Number: K872780 · Decision Oct 6, 1987
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
70
Applicant Total
1
Review Days
84

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
GUS TRAC C-303
K Number
K872780
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5900
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Gus Company, Inc.
Date Received
July 14, 1987
Decision Date
October 6, 1987
Product Code
ITH
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
ITH Equipment, Traction, Powered

Similar 510(k) Clearances

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

View all