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FDA 510(k)

RICHTER MALE LATEX CONDOM

K-Number: K070511 · 2008-01-14

Decision Date2008-01-14
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RICHTER MALE LATEX CONDOM is the device name listed in this FDA 510(k) record. The listed applicant is Richter Rubber Technology Sbn Bhd. It received FDA 510(k) clearance on 2008-01-14 under 510(k) number K070511. 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 RICHTER MALE LATEX CONDOM?

RICHTER MALE LATEX CONDOM is a medical device that received FDA 510(k) clearance on 2008-01-14. The listed applicant is Richter Rubber Technology Sbn Bhd. The 510(k) number is K070511.

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

RICHTER MALE LATEX CONDOM received FDA 510(k) clearance on 2008-01-14, under 510(k) number K070511.

Who is the listed applicant for RICHTER MALE LATEX CONDOM?

The FDA 510(k) record lists Richter Rubber Technology Sbn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RICHTER MALE LATEX CONDOM?

The FDA product code for RICHTER MALE LATEX CONDOM 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.

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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