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

DELUXE KNEE IMMOBILIZER(UNIVERSAL)

K Number: K823658 · Decision Dec 30, 1982
Classifications
1
FEI Numbers
442
Registration Numbers
442
Same Product Code
14
Applicant Total
24
Review Days
24

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Basic Information

Device Name
DELUXE KNEE IMMOBILIZER(UNIVERSAL)
K Number
K823658
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3475
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Warm & Form, Orthopedic Materials
Date Received
December 6, 1982
Decision Date
December 30, 1982
Product Code
ITQ
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
ITQ Joint, Knee, External Brace

Similar 510(k) Clearances

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

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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
K823660 UNIVERSAL BUCKS TRACTION
K823662 RIB BELT (UNIVERSAL)
K823664 UNIVERSAL SLING, SLING & SWATHE
K823666 UNIVERSAL WRIST SPLINT & FOREARM SPLINT
K823663 ABDOMINAL BINDER
Search all 24 clearances from Warm & Form, Orthopedic Materials →