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

ACCUFLEX DYNAMIC ELBOW ORTHOSIS

K Number: K926391 · Decision Jul 22, 1993
Classifications
1
FEI Numbers
503
Registration Numbers
503
Same Product Code
51
Applicant Total
21
Review Days
213

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Basic Information

Device Name
ACCUFLEX DYNAMIC ELBOW ORTHOSIS
K Number
K926391
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3475
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Regulatory & Marketing Services, Inc.
Date Received
December 21, 1992
Decision Date
July 22, 1993
Product Code
IQI
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
IQI Orthosis, Limb Brace

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K941543 DIAL MEDICAL KIT
K944378 ORION'S URETHRAL CATHETERIZATION KIT WITH CATHETER AND BAG
K944384 ORION'S URETHRAL CATHETERIZATION KIT WITHOUT BAG
K944379 ORION'S FOLEY CATHETERIZATION KIT WITH CATHETER AND BAG
K945874 EUROMEDICAL POLY TRACHEOTOMY TUBE
K944383 ORION RED URETHRAL CATHETER
K944382 ORION ALL SILICONE FOLEY CATHETER
Search all 21 clearances from Regulatory & Marketing Services, Inc. →