LUBRICATED BAGGY TACTYLON CONDOM
K-Number: K974121 · 1998-01-29
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Device Summary
Frequently Asked Questions
What is the LUBRICATED BAGGY TACTYLON CONDOM?
LUBRICATED BAGGY TACTYLON CONDOM is a medical device that received FDA 510(k) clearance on 1998-01-29. The listed applicant is Sensicon Corp.. The 510(k) number is K974121.
When did LUBRICATED BAGGY TACTYLON CONDOM receive FDA 510(k) clearance?
LUBRICATED BAGGY TACTYLON CONDOM received FDA 510(k) clearance on 1998-01-29, under 510(k) number K974121.
Who is the listed applicant for LUBRICATED BAGGY TACTYLON CONDOM?
The FDA 510(k) record lists Sensicon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUBRICATED BAGGY TACTYLON CONDOM?
The FDA product code for LUBRICATED BAGGY TACTYLON CONDOM is MOL.
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 Sensicon Corp. 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: MOL)
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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