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FDA 510(k)

OVAMED INTRAUTERINE ACCESS CATHETER

K-Number: K931534 · 1995-07-28

ApplicantOvamed Corp.
Decision Date1995-07-28
Product CodeMOV
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OVAMED INTRAUTERINE ACCESS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Ovamed Corp.. It received FDA 510(k) clearance on 1995-07-28 under 510(k) number K931534. 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 OVAMED INTRAUTERINE ACCESS CATHETER?

OVAMED INTRAUTERINE ACCESS CATHETER is a medical device that received FDA 510(k) clearance on 1995-07-28. The listed applicant is Ovamed Corp.. The 510(k) number is K931534.

When did OVAMED INTRAUTERINE ACCESS CATHETER receive FDA 510(k) clearance?

OVAMED INTRAUTERINE ACCESS CATHETER received FDA 510(k) clearance on 1995-07-28, under 510(k) number K931534.

Who is the listed applicant for OVAMED INTRAUTERINE ACCESS CATHETER?

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

What is the FDA product code for OVAMED INTRAUTERINE ACCESS CATHETER?

The FDA product code for OVAMED INTRAUTERINE ACCESS CATHETER is MOV.

Related Clinical Trials

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.

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Other records listing Ovamed Corp. 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.

K951946HYSTEROSYS FLEXIBLE HYSTEROCOPEK931167OVAMED FALLOPIAN OSTIAL ACCESS CATHETERK943593SARATOGA MODULAR MINIATURE ENDOSCOPE SYSTEMK931122OVAMED HSG CATHETER

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.K953314CONCEPTUS FALLOPIAN TUBE CATHETERIZATION SYSTEMConceptus, Inc.K931476NOVY CORNUAL CANNULATION SETCook Ob/Gyn

Official Source

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

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