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FDA 510(k)

EER ERECTION ENHANCED RESPONDER

K-Number: K904406 · 1991-02-25

ApplicantEer, Inc.
Decision Date1991-02-25
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EER ERECTION ENHANCED RESPONDER is the device name listed in this FDA 510(k) record. The listed applicant is Eer, Inc.. It received FDA 510(k) clearance on 1991-02-25 under 510(k) number K904406. 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 EER ERECTION ENHANCED RESPONDER?

EER ERECTION ENHANCED RESPONDER is a medical device that received FDA 510(k) clearance on 1991-02-25. The listed applicant is Eer, Inc.. The 510(k) number is K904406.

When did EER ERECTION ENHANCED RESPONDER receive FDA 510(k) clearance?

EER ERECTION ENHANCED RESPONDER received FDA 510(k) clearance on 1991-02-25, under 510(k) number K904406.

Who is the listed applicant for EER ERECTION ENHANCED RESPONDER?

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

What is the FDA product code for EER ERECTION ENHANCED RESPONDER?

The FDA product code for EER ERECTION ENHANCED RESPONDER 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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