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FDA 510(k)

BLAUSIEGEL TRANSPARENT CONDOMS

K-Number: K871267 · 1988-04-12

ApplicantTicosan, Inc.
Decision Date1988-04-12
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BLAUSIEGEL TRANSPARENT CONDOMS is the device name listed in this FDA 510(k) record. The listed applicant is Ticosan, Inc.. It received FDA 510(k) clearance on 1988-04-12 under 510(k) number K871267. The device is classified under product code HIS. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLAUSIEGEL TRANSPARENT CONDOMS?

BLAUSIEGEL TRANSPARENT CONDOMS is a medical device that received FDA 510(k) clearance on 1988-04-12. The listed applicant is Ticosan, Inc.. The 510(k) number is K871267.

When did BLAUSIEGEL TRANSPARENT CONDOMS receive FDA 510(k) clearance?

BLAUSIEGEL TRANSPARENT CONDOMS received FDA 510(k) clearance on 1988-04-12, under 510(k) number K871267.

Who is the listed applicant for BLAUSIEGEL TRANSPARENT CONDOMS?

The FDA 510(k) record lists Ticosan, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLAUSIEGEL TRANSPARENT CONDOMS?

The FDA product code for BLAUSIEGEL TRANSPARENT 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

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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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