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FDA 510(k)

VED VALU- VACUUM ERECTION DEVICE

K-Number: K980948 · 1998-06-25

Decision Date1998-06-25
Product CodeLKY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VED VALU- VACUUM ERECTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Mission Pharmacal Comp. It received FDA 510(k) clearance on 1998-06-25 under 510(k) number K980948. 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 VED VALU- VACUUM ERECTION DEVICE?

VED VALU- VACUUM ERECTION DEVICE is a medical device that received FDA 510(k) clearance on 1998-06-25. The listed applicant is Mission Pharmacal Comp. The 510(k) number is K980948.

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

VED VALU- VACUUM ERECTION DEVICE received FDA 510(k) clearance on 1998-06-25, under 510(k) number K980948.

Who is the listed applicant for VED VALU- VACUUM ERECTION DEVICE?

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

What is the FDA product code for VED VALU- VACUUM ERECTION DEVICE?

The FDA product code for VED VALU- VACUUM ERECTION 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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