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FDA 510(k)

CONSTRICTOR RING FOR PENILE ERECTION

K-Number: K891125 · 1989-04-27

Decision Date1989-04-27
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CONSTRICTOR RING FOR PENILE ERECTION is the device name listed in this FDA 510(k) record. The listed applicant is Performance, Inc.. It received FDA 510(k) clearance on 1989-04-27 under 510(k) number K891125. 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 CONSTRICTOR RING FOR PENILE ERECTION?

CONSTRICTOR RING FOR PENILE ERECTION is a medical device that received FDA 510(k) clearance on 1989-04-27. The listed applicant is Performance, Inc.. The 510(k) number is K891125.

When did CONSTRICTOR RING FOR PENILE ERECTION receive FDA 510(k) clearance?

CONSTRICTOR RING FOR PENILE ERECTION received FDA 510(k) clearance on 1989-04-27, under 510(k) number K891125.

Who is the listed applicant for CONSTRICTOR RING FOR PENILE ERECTION?

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

What is the FDA product code for CONSTRICTOR RING FOR PENILE ERECTION?

The FDA product code for CONSTRICTOR RING FOR PENILE ERECTION 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.

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.

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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