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

TUBULAR DRESSING RETAINER

K Number: K780570 · Decision Apr 19, 1978
Classifications
1
FEI Numbers
681
Registration Numbers
681
Same Product Code
41
Applicant Total
8
Review Days
9

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Basic Information

Device Name
TUBULAR DRESSING RETAINER
K Number
K780570
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5075
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Alba-Waldensian, Inc.
Date Received
April 10, 1978
Decision Date
April 19, 1978
Product Code
FQM
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
FQM Bandage, Elastic

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K792357 STERILE IMPERVIOUS ORTHOPEDIC STOCKIN
K781964 COMPRESSION DEVICES, LIMB
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K771913 HEEL/ELBOW PROTECTOR