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FDA 510(k)

SAFE AID DEVICE IMPOTENCE DEVICE

K-Number: K896357 · 1990-04-25

Decision Date1990-04-25
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SAFE AID DEVICE IMPOTENCE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Dr. John P. March. It received FDA 510(k) clearance on 1990-04-25 under 510(k) number K896357. 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 SAFE AID DEVICE IMPOTENCE DEVICE?

SAFE AID DEVICE IMPOTENCE DEVICE is a medical device that received FDA 510(k) clearance on 1990-04-25. The listed applicant is Dr. John P. March. The 510(k) number is K896357.

When did SAFE AID DEVICE IMPOTENCE DEVICE receive FDA 510(k) clearance?

SAFE AID DEVICE IMPOTENCE DEVICE received FDA 510(k) clearance on 1990-04-25, under 510(k) number K896357.

Who is the listed applicant for SAFE AID DEVICE IMPOTENCE DEVICE?

The FDA 510(k) record lists Dr. John P. March as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAFE AID DEVICE IMPOTENCE DEVICE?

The FDA product code for SAFE AID DEVICE IMPOTENCE DEVICE 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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