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FDA 510(k)

CONCEIVEX LATEX-FREE SEMEN COLLECTOR

K-Number: K080752 · 2008-05-14

ApplicantConceivex, Inc.
Decision Date2008-05-14
Product CodeOBB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CONCEIVEX LATEX-FREE SEMEN COLLECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Conceivex, Inc.. It received FDA 510(k) clearance on 2008-05-14 under 510(k) number K080752. The device is classified under product code OBB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONCEIVEX LATEX-FREE SEMEN COLLECTOR?

CONCEIVEX LATEX-FREE SEMEN COLLECTOR is a medical device that received FDA 510(k) clearance on 2008-05-14. The listed applicant is Conceivex, Inc.. The 510(k) number is K080752.

When did CONCEIVEX LATEX-FREE SEMEN COLLECTOR receive FDA 510(k) clearance?

CONCEIVEX LATEX-FREE SEMEN COLLECTOR received FDA 510(k) clearance on 2008-05-14, under 510(k) number K080752.

Who is the listed applicant for CONCEIVEX LATEX-FREE SEMEN COLLECTOR?

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

What is the FDA product code for CONCEIVEX LATEX-FREE SEMEN COLLECTOR?

The FDA product code for CONCEIVEX LATEX-FREE SEMEN COLLECTOR is OBB.

Related Clinical Trials

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Other records listing Conceivex, 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.

K063227CONCEIVEX CONCEPTION KIT

Related Devices (Code: OBB)

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.

K112200FOCUS TOUCH CONCEPTION SYSTEMIntimate Bridge 2 Conception, Inc.K063227CONCEIVEX CONCEPTION KITConceivex, Inc.

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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