LUBRICATED CONDOM
K-Number: K953583 · 1996-01-26
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Device Summary
Frequently Asked Questions
What is the LUBRICATED CONDOM?
LUBRICATED CONDOM is a medical device that received FDA 510(k) clearance on 1996-01-26. The listed applicant is Tactyl Technologies, Inc.. The 510(k) number is K953583.
When did LUBRICATED CONDOM receive FDA 510(k) clearance?
LUBRICATED CONDOM received FDA 510(k) clearance on 1996-01-26, under 510(k) number K953583.
Who is the listed applicant for LUBRICATED CONDOM?
The FDA 510(k) record lists Tactyl Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUBRICATED CONDOM?
The FDA product code for LUBRICATED CONDOM is HIS.
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 Tactyl Technologies, 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: HIS)
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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