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

MICROSURGE THORACOSCOPIC ACCESS SYSTEM

K Number: K953121 · Decision Sep 29, 1995
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
15
Review Days
86

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Basic Information

Device Name
MICROSURGE THORACOSCOPIC ACCESS SYSTEM
K Number
K953121
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Microsurge, Inc.
Date Received
July 5, 1995
Decision Date
September 29, 1995
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
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
GCJ Laparoscope, General & Plastic Surgery

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K954641 ENDO-LEADER
K954072 MICROSURGE PUNCTURE CLOSE DEVICE
K954520 MICROSURGE VERESS NEEDLE
K951230 MICROSURGE BIPOLAR GRASPERS
K933750 MICROSURGE REUSABLE FRONT END GRASP DEVICES, MODIF
K930355 MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS
K925830 MICROSURGE SUCTION/IRRIGATION SYSTEM
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