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

TAYLOR PATIENT TRANSFER BOARD

K Number: K792247 · Decision Nov 30, 1979
Classifications
1
FEI Numbers
282
Registration Numbers
282
Same Product Code
17
Applicant Total
2
Review Days
23

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
TAYLOR PATIENT TRANSFER BOARD
K Number
K792247
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5050
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Taylor Medical Equipment
Date Received
November 7, 1979
Decision Date
November 30, 1979
Product Code
IKX
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
IKX Aid, Transfer

Similar 510(k) Clearances

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

View all

Other Clearances by Taylor Medical Equipment

K Number Device Name
K792248 TAYLOR TRACTION CORD