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FDA 510(k)

CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM

K-Number: K953314 · 1995-07-28

ApplicantConceptus, Inc.
Decision Date1995-07-28
Product CodeMOV
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Conceptus, Inc.. It received FDA 510(k) clearance on 1995-07-28 under 510(k) number K953314. The device is classified under product code MOV. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM?

CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM is a medical device that received FDA 510(k) clearance on 1995-07-28. The listed applicant is Conceptus, Inc.. The 510(k) number is K953314.

When did CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM receive FDA 510(k) clearance?

CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM received FDA 510(k) clearance on 1995-07-28, under 510(k) number K953314.

Who is the listed applicant for CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM?

The FDA 510(k) record lists Conceptus, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM?

The FDA product code for CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEM is MOV.

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Other records listing Conceptus, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K974028STARGATE FALLOPOSCOPY CATHETER, TRIFURCATED IRRIGATION TUBINGK972210RESECTOSCOPE SAFETY SHEATHK962587CONCEPTUS FALLOPIAN TUBE CATHETEIZATION WITH MICROENDOSCOPY SYSTEMK954164HYSTEROSCOPEK932387CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDRELK932993INTRAUTERINE CATHETER AND INTRODUCER

View all 9 devices →

Related Devices (Code: MOV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K180552Modified Novy Cornual Cannulation SetCook IncorporatedK932436ECHOMARK INTRAUTERINE GUIDING CATHETEREchocath, Inc.K931534OVAMED INTRAUTERINE ACCESS CATHETEROvamed Corp.K931476NOVY CORNUAL CANNULATION SETCook Ob/Gyn

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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