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FDA 510(k)

CONCEIVEX CONCEPTION KIT

K-Number: K063227 · 2007-03-14

ApplicantConceivex, Inc.
Decision Date2007-03-14
Product CodeOBB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CONCEIVEX CONCEPTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Conceivex, Inc.. It received FDA 510(k) clearance on 2007-03-14 under 510(k) number K063227. 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 CONCEPTION KIT?

CONCEIVEX CONCEPTION KIT is a medical device that received FDA 510(k) clearance on 2007-03-14. The listed applicant is Conceivex, Inc.. The 510(k) number is K063227.

When did CONCEIVEX CONCEPTION KIT receive FDA 510(k) clearance?

CONCEIVEX CONCEPTION KIT received FDA 510(k) clearance on 2007-03-14, under 510(k) number K063227.

Who is the listed applicant for CONCEIVEX CONCEPTION KIT?

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 CONCEPTION KIT?

The FDA product code for CONCEIVEX CONCEPTION KIT is OBB.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K080752CONCEIVEX LATEX-FREE SEMEN COLLECTOR

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.K080752CONCEIVEX LATEX-FREE SEMEN COLLECTORConceivex, Inc.

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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