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FDA 510(k)

INTRAUTERINE CATHETER AND INTRODUCER

K-Number: K932993 · 1995-01-06

ApplicantConceptus, Inc.
Decision Date1995-01-06
Product CodeMFD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INTRAUTERINE CATHETER AND INTRODUCER is the device name listed in this FDA 510(k) record. The listed applicant is Conceptus, Inc.. It received FDA 510(k) clearance on 1995-01-06 under 510(k) number K932993. The device is classified under product code MFD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRAUTERINE CATHETER AND INTRODUCER?

INTRAUTERINE CATHETER AND INTRODUCER is a medical device that received FDA 510(k) clearance on 1995-01-06. The listed applicant is Conceptus, Inc.. The 510(k) number is K932993.

When did INTRAUTERINE CATHETER AND INTRODUCER receive FDA 510(k) clearance?

INTRAUTERINE CATHETER AND INTRODUCER received FDA 510(k) clearance on 1995-01-06, under 510(k) number K932993.

Who is the listed applicant for INTRAUTERINE CATHETER AND INTRODUCER?

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 INTRAUTERINE CATHETER AND INTRODUCER?

The FDA product code for INTRAUTERINE CATHETER AND INTRODUCER is MFD.

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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 SYSTEMK954164HYSTEROSCOPEK953314CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEMK932387CONCEPTUS VARI-SOFT CATH/PIROUETTE POSIT MANDREL

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Related Devices (Code: MFD)

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.

K021438INSEMINATION CATHETER, MODEL 320301Labotect Labor-Technik GottingenK012935THECURVE, ITEM 507Select Medical Systems, Inc.K984306`THE INSEMINATOR' (PROPOSED)Wallach Surgical Devices, Inc.K982630MEDWORKS VISUALIZATION INSEMINATION CATHETERMedworks Corp.K982628MEDWORKS INSEMINATION CATHETERMedworks Corp.K980061EMBRYON INTRAUTERINE INSEMINATION CATHETER, EMRYON SOFT INTRAUTERINE INSEMINATION CATHETER, STYLET FOR EMBRYON INTRAUTERRocket Medical Plc

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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