FYH · Class I · 21 CFR 878.3910

FDA Product Code FYH: Splint, Extremity, Noninflatable, External, Sterile

Leading manufacturers include Johnson & Johnson Professionals, Inc., Orthopedic Systems, Inc. and The Huxley Instrument Corp..

8
Total
8
Cleared
71d
Avg days
1980
Since

FDA 510(k) Cleared Splint, Extremity, Noninflatable, External, Sterile Devices (Product Code FYH)

8 devices
1–8 of 8
Cleared Jul 02, 1985
SPLINTS(ALL TYPE)
K852558
The Huxley Instrument Corp.
General Hospital · 15d
Cleared Jul 02, 1982
J & J DIP WATER ADDITIVE
K821693
Johnson & Johnson Professionals, Inc.
General Hospital · 24d
Cleared Jan 08, 1981
DELTA-LITE CASTING TAPE & SPLINTS
K802522
Johnson & Johnson Professionals, Inc.
General Hospital · 85d
Cleared Jun 26, 1980
ORTHOPEDIC LOWER EXTREMITY SUSPENSION
K801436
Orthopedic Systems, Inc.
General Hospital · 7d

About Product Code FYH - Regulatory Context