VET (VACUUM ERECTION TECHNOLOGY)
K-Number: K902240 · 1990-10-12
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Device Summary
Frequently Asked Questions
What is the VET (VACUUM ERECTION TECHNOLOGY)?
VET (VACUUM ERECTION TECHNOLOGY) is a medical device that received FDA 510(k) clearance on 1990-10-12. The listed applicant is Vetco, Inc.. The 510(k) number is K902240.
When did VET (VACUUM ERECTION TECHNOLOGY) receive FDA 510(k) clearance?
VET (VACUUM ERECTION TECHNOLOGY) received FDA 510(k) clearance on 1990-10-12, under 510(k) number K902240.
Who is the listed applicant for VET (VACUUM ERECTION TECHNOLOGY)?
The FDA 510(k) record lists Vetco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VET (VACUUM ERECTION TECHNOLOGY)?
The FDA product code for VET (VACUUM ERECTION TECHNOLOGY) 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.
Other records listing Vetco, Inc. 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.
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
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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