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FDA 510(k)

VACUUM ERECTION DEVICE (VED)

K-Number: K901223 · 1990-05-04

ApplicantMission Pharmacal Co.
Decision Date1990-05-04
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VACUUM ERECTION DEVICE (VED) is the device name listed in this FDA 510(k) record. The listed applicant is Mission Pharmacal Co.. It received FDA 510(k) clearance on 1990-05-04 under 510(k) number K901223. The device is classified under product code LKY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VACUUM ERECTION DEVICE (VED)?

VACUUM ERECTION DEVICE (VED) is a medical device that received FDA 510(k) clearance on 1990-05-04. The listed applicant is Mission Pharmacal Co.. The 510(k) number is K901223.

When did VACUUM ERECTION DEVICE (VED) receive FDA 510(k) clearance?

VACUUM ERECTION DEVICE (VED) received FDA 510(k) clearance on 1990-05-04, under 510(k) number K901223.

Who is the listed applicant for VACUUM ERECTION DEVICE (VED)?

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

What is the FDA product code for VACUUM ERECTION DEVICE (VED)?

The FDA product code for VACUUM ERECTION DEVICE (VED) is LKY.

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 Mission Pharmacal Co. 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.

K943010MAXILUBEK843382UROCYSTIN

Related Devices (Code: LKY)

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.

K041573NANMA VACUUM PUMP PROXZEK MODEL 2M9498SNanma Mfg Co., Ltd.K032776VACURECT VACUUM CONSTRICTION DEVICEVacurect Manufacturing (Pty) , Ltd.K030119NANMA ADJUSTABLE CONSTRICTION RINGNanma Mfg Co., Ltd.K030913NANMA VACUUM PUMPNanma Mfg Co., Ltd.K013113MODIFICATION TO NANMA VACUUM PUMPNanma Mfg Co., Ltd.K013051NANMA ADJUSTABLE CONSTRICTION RINGNanma Mfg Co., Ltd.

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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