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FDA 510(k)

RUBBER CONTRACEPTIVE

K-Number: K896107 · 1990-06-29

ApplicantBanrub Sdn Bhd
Decision Date1990-06-29
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RUBBER CONTRACEPTIVE is the device name listed in this FDA 510(k) record. The listed applicant is Banrub Sdn Bhd. It received FDA 510(k) clearance on 1990-06-29 under 510(k) number K896107. 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 RUBBER CONTRACEPTIVE?

RUBBER CONTRACEPTIVE is a medical device that received FDA 510(k) clearance on 1990-06-29. The listed applicant is Banrub Sdn Bhd. The 510(k) number is K896107.

When did RUBBER CONTRACEPTIVE receive FDA 510(k) clearance?

RUBBER CONTRACEPTIVE received FDA 510(k) clearance on 1990-06-29, under 510(k) number K896107.

Who is the listed applicant for RUBBER CONTRACEPTIVE?

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

What is the FDA product code for RUBBER CONTRACEPTIVE?

The FDA product code for RUBBER CONTRACEPTIVE is HIS.

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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.

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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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