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

ABDOMINAL BINDER

K Number: K823663 · Decision Dec 30, 1982
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
2
Applicant Total
24
Review Days
24

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Basic Information

Device Name
ABDOMINAL BINDER
K Number
K823663
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3490
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Warm & Form, Orthopedic Materials
Date Received
December 6, 1982
Decision Date
December 30, 1982
Product Code
KTD
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
KTD Orthosis, Abdominal

Similar 510(k) Clearances

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Other Clearances by Warm & Form, Orthopedic Materials

K Number Device Name
K830244 TRACTION ACCESSORIES
K830245 HEAD HALTER
K830243 ABDUCTION PILLOW
K830246 CAST SHOE, CAST BOOT
K823659 PELVIC TRACTION BELT
K823658 DELUXE KNEE IMMOBILIZER(UNIVERSAL)
K823660 UNIVERSAL BUCKS TRACTION
K823662 RIB BELT (UNIVERSAL)
K823664 UNIVERSAL SLING, SLING & SWATHE
K823666 UNIVERSAL WRIST SPLINT & FOREARM SPLINT
Search all 24 clearances from Warm & Form, Orthopedic Materials →