DUET (CONDOMS)
K-Number: K880185 · 1988-06-17
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Device Summary
Frequently Asked Questions
What is the DUET (CONDOMS)?
DUET (CONDOMS) is a medical device that received FDA 510(k) clearance on 1988-06-17. The listed applicant is American Laboratories, Inc.. The 510(k) number is K880185.
When did DUET (CONDOMS) receive FDA 510(k) clearance?
DUET (CONDOMS) received FDA 510(k) clearance on 1988-06-17, under 510(k) number K880185.
Who is the listed applicant for DUET (CONDOMS)?
The FDA 510(k) record lists American Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DUET (CONDOMS)?
The FDA product code for DUET (CONDOMS) 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.
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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