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FDA 510(k)

ANGEL LATEX PROPHYLACTICS (CONDOMS)

K-Number: K871948 · 1987-10-20

Decision Date1987-10-20
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ANGEL LATEX PROPHYLACTICS (CONDOMS) is the device name listed in this FDA 510(k) record. The listed applicant is Angel Intl. Trading Co., Inc.. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K871948. 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 ANGEL LATEX PROPHYLACTICS (CONDOMS)?

ANGEL LATEX PROPHYLACTICS (CONDOMS) is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Angel Intl. Trading Co., Inc.. The 510(k) number is K871948.

When did ANGEL LATEX PROPHYLACTICS (CONDOMS) receive FDA 510(k) clearance?

ANGEL LATEX PROPHYLACTICS (CONDOMS) received FDA 510(k) clearance on 1987-10-20, under 510(k) number K871948.

Who is the listed applicant for ANGEL LATEX PROPHYLACTICS (CONDOMS)?

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

What is the FDA product code for ANGEL LATEX PROPHYLACTICS (CONDOMS)?

The FDA product code for ANGEL LATEX PROPHYLACTICS (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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