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

MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS

K Number: K930355 · Decision Jun 8, 1993
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
15
Review Days
134

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Basic Information

Device Name
MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS
K Number
K930355
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Microsurge, Inc.
Date Received
January 25, 1993
Decision Date
June 8, 1993
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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K954072 MICROSURGE PUNCTURE CLOSE DEVICE
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K953121 MICROSURGE THORACOSCOPIC ACCESS SYSTEM
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K925830 MICROSURGE SUCTION/IRRIGATION SYSTEM
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