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FDA 510(k)

PREVENTOR AND PROTECTOR LATEX CONDOMS

K-Number: K945246 · 1995-09-07

Decision Date1995-09-07
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PREVENTOR AND PROTECTOR LATEX CONDOMS is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaceutical Co., Inc.. It received FDA 510(k) clearance on 1995-09-07 under 510(k) number K945246. 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 PREVENTOR AND PROTECTOR LATEX CONDOMS?

PREVENTOR AND PROTECTOR LATEX CONDOMS is a medical device that received FDA 510(k) clearance on 1995-09-07. The listed applicant is American Pharmaceutical Co., Inc.. The 510(k) number is K945246.

When did PREVENTOR AND PROTECTOR LATEX CONDOMS receive FDA 510(k) clearance?

PREVENTOR AND PROTECTOR LATEX CONDOMS received FDA 510(k) clearance on 1995-09-07, under 510(k) number K945246.

Who is the listed applicant for PREVENTOR AND PROTECTOR LATEX CONDOMS?

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

What is the FDA product code for PREVENTOR AND PROTECTOR LATEX CONDOMS?

The FDA product code for PREVENTOR AND PROTECTOR LATEX 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.

Other records listing American Pharmaceutical Co., 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

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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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