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FDA 510(k)

MALE LATEX CONDOM 56MM

K-Number: K994312 · 2000-03-21

Decision Date2000-03-21
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MALE LATEX CONDOM 56MM is the device name listed in this FDA 510(k) record. The listed applicant is Pleasure Latex Products Sdn. Bhd.. It received FDA 510(k) clearance on 2000-03-21 under 510(k) number K994312. 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 MALE LATEX CONDOM 56MM?

MALE LATEX CONDOM 56MM is a medical device that received FDA 510(k) clearance on 2000-03-21. The listed applicant is Pleasure Latex Products Sdn. Bhd.. The 510(k) number is K994312.

When did MALE LATEX CONDOM 56MM receive FDA 510(k) clearance?

MALE LATEX CONDOM 56MM received FDA 510(k) clearance on 2000-03-21, under 510(k) number K994312.

Who is the listed applicant for MALE LATEX CONDOM 56MM?

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

What is the FDA product code for MALE LATEX CONDOM 56MM?

The FDA product code for MALE LATEX CONDOM 56MM 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 Pleasure Latex Products Sdn. Bhd. 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 10 devices →

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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