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FDA 510(k)

DUREX, RAMSES, SHEIK

K-Number: K952415 · 1996-07-15

ApplicantLondon International U.S. Holdings, Inc.
Decision Date1996-07-15
Product CodeLTZ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DUREX, RAMSES, SHEIK 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 1996-07-15 under 510(k) number K952415. 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 DUREX, RAMSES, SHEIK?

DUREX, RAMSES, SHEIK is a medical device that received FDA 510(k) clearance on 1996-07-15. The listed applicant is London International U.S. Holdings, Inc.. The 510(k) number is K952415.

When did DUREX, RAMSES, SHEIK receive FDA 510(k) clearance?

DUREX, RAMSES, SHEIK received FDA 510(k) clearance on 1996-07-15, under 510(k) number K952415.

Who is the listed applicant for DUREX, RAMSES, SHEIK?

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 DUREX, RAMSES, SHEIK?

The FDA product code for DUREX, RAMSES, SHEIK is LTZ.

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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.

K953813LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS

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Official Source

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