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FDA 510(k)

LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS

K-Number: K953813 · 1996-07-22

Decision Date1996-07-22
Product CodeLTZ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS is the device name listed in this FDA 510(k) record. The listed applicant is London International U.S. Holdings, Inc.. It received FDA 510(k) clearance on 1996-07-22 under 510(k) number K953813. 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 LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS?

LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS is a medical device that received FDA 510(k) clearance on 1996-07-22. The listed applicant is London International U.S. Holdings, Inc.. The 510(k) number is K953813.

When did LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS receive FDA 510(k) clearance?

LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS received FDA 510(k) clearance on 1996-07-22, under 510(k) number K953813.

Who is the listed applicant for LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS?

The FDA 510(k) record lists London International U.S. Holdings, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS?

The FDA product code for LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS 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 London International U.S. Holdings, 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: 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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