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

3000 ELECTRONIC INSUFFLATOR MODIFICATION

K Number: K934115 · Decision Mar 15, 1995
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
176
Applicant Total
38
Review Days
568

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Basic Information

Device Name
3000 ELECTRONIC INSUFFLATOR MODIFICATION
K Number
K934115
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1730
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cabot Medical Corp.
Date Received
August 24, 1993
Decision Date
March 15, 1995
Product Code
HIF
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
HIF Insufflator, Laparoscopic

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K930954 THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV
K932626 CABOT MEDICAL SURGIFLEX(R) SUCTION-IRRIGATION PROB
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K924631 CABOT MEDICAL UTERINE RESECTOSCOPE
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