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

HEEL OR ELBOW PROTECTOR

K Number: K812344 · Decision Sep 11, 1981
Classifications
1
FEI Numbers
374
Registration Numbers
374
Same Product Code
22
Applicant Total
278
Review Days
24

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
HEEL OR ELBOW PROTECTOR
K Number
K812344
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6450
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Fred Sammons, Inc.
Date Received
August 18, 1981
Decision Date
September 11, 1981
Product Code
FMP
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FMP Protector, Skin Pressure

Similar 510(k) Clearances

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

View all

Other Clearances by Fred Sammons, Inc.

K Number Device Name
K880644 ULTRA-PAN FOR ORTHOTIC PLASTICS (7262)
K880647 ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)
K831549 ARM SLINGS
K831548 SPLINTS
K831542 ADJUSTABLE POLYCENTRIC ELBOW HINGE
K831550 FINGER BONIOMETER BK7506
K831543 ADJUST. WEIGHTS-BK5171-05,10,20 BEOK
K831544 DELUXE TRACTION EXERCISE GLOVE BK5035
K831553 LEG DRAINAGE BAG STRAP BK6011
K831547 RAISED TOILET SEATS & NAIL CLIPPERS
Search all 278 clearances from Fred Sammons, Inc. →