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FDA 510(k)

MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB.

K-Number: K904273 · 1990-10-31

Decision Date1990-10-31
Product CodeLTZ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB. is the device name listed in this FDA 510(k) record. The listed applicant is Carter Products. It received FDA 510(k) clearance on 1990-10-31 under 510(k) number K904273. The device is classified under product code LTZ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB.?

MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB. is a medical device that received FDA 510(k) clearance on 1990-10-31. The listed applicant is Carter Products. The 510(k) number is K904273.

When did MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB. receive FDA 510(k) clearance?

MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB. received FDA 510(k) clearance on 1990-10-31, under 510(k) number K904273.

Who is the listed applicant for MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB.?

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

What is the FDA product code for MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB.?

The FDA product code for MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB. is LTZ.

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 Carter Products 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.

View all 20 devices →

Related Devices (Code: LTZ)

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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