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

MICROSURGE VERESS NEEDLE

K Number: K954520 · Decision Oct 16, 1995
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
337
Applicant Total
15
Review Days
18

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Basic Information

Device Name
MICROSURGE VERESS NEEDLE
K Number
K954520
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1720
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Microsurge, Inc.
Date Received
September 28, 1995
Decision Date
October 16, 1995
Product Code
HET
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HET Laparoscope, Gynecologic (And Accessories)

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K953121 MICROSURGE THORACOSCOPIC ACCESS SYSTEM
K951230 MICROSURGE BIPOLAR GRASPERS
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K930355 MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS
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