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FDA 510(k)

LI VASECTOMY

K-Number: K932465 · 1994-03-02

ApplicantFemcare , Ltd.
Decision Date1994-03-02
Product CodeKOA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LI VASECTOMY is the device name listed in this FDA 510(k) record. The listed applicant is Femcare , Ltd.. It received FDA 510(k) clearance on 1994-03-02 under 510(k) number K932465. The device is classified under product code KOA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LI VASECTOMY?

LI VASECTOMY is a medical device that received FDA 510(k) clearance on 1994-03-02. The listed applicant is Femcare , Ltd.. The 510(k) number is K932465.

When did LI VASECTOMY receive FDA 510(k) clearance?

LI VASECTOMY received FDA 510(k) clearance on 1994-03-02, under 510(k) number K932465.

Who is the listed applicant for LI VASECTOMY?

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

What is the FDA product code for LI VASECTOMY?

The FDA product code for LI VASECTOMY is KOA.

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 Femcare , Ltd. 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.

K884061ADD-A-CATH

Related Devices (Code: KOA)

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.

K182664FiXcisionAgency For Medical Innovations GmbHK950267URETHRAL SUTURE GUIDEApplied Medical ResourcesK921546VASOVASOSTOMY SETCook Urological, Inc.K931181VESITEC SUTURE PASSERVesitec Medical, Inc.K921304DDV LIGATORNorth American Medical, Inc.K922971NO-SCALPEL VASCETOMY INSTRUMENTSPilling Co.

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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