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

THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV

K Number: K930954 · Decision Jun 30, 1994
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
71
Applicant Total
38
Review Days
492

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Basic Information

Device Name
THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV
K Number
K930954
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cabot Medical Corp.
Date Received
February 23, 1993
Decision Date
June 30, 1994
Product Code
HIB
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
HIB Speculum, Vaginal, Nonmetal

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K941743 CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMP
K934115 3000 ELECTRONIC INSUFFLATOR MODIFICATION
K932293 CABOT MEDICAL BIPOLAR CUTTING FORCEPS
K932626 CABOT MEDICAL SURGIFLEX(R) SUCTION-IRRIGATION PROB
K935786 CORSON AND NEZHAT SUCTION/IRRIGATION PROBES
K924631 CABOT MEDICAL UTERINE RESECTOSCOPE
Search all 38 clearances from Cabot Medical Corp. →