FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AUTO-CLIP

K Number: K771021 · Decision Jun 14, 1977
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
7
Applicant Total
28
Review Days
8

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Basic Information

Device Name
AUTO-CLIP
K Number
K771021
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Axiom Medical, Inc.
Date Received
June 6, 1977
Decision Date
June 14, 1977
Product Code
DSS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DSS Clip, Vascular

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K934895 GLASSMAN SILICONE CATHETER
K922760 ATRAUM WOUND DRESSING--MODIFICATION
K905422 PVC ROUND WOUND DRAINS
K904218 SUCTION SYSTEM
K904133 DISPOSABLE FLUID COLLECTION BAG
K863247 AXIOM TROCAR THORACIC CATHETER
K861306 SUCTION SYSTEM
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