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FDA 510(k)

INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED

K-Number: K000039 · 2000-03-21

ApplicantIndus Medicare , Ltd.
Decision Date2000-03-21
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED is the device name listed in this FDA 510(k) record. The listed applicant is Indus Medicare , Ltd.. It received FDA 510(k) clearance on 2000-03-21 under 510(k) number K000039. 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 INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED?

INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED is a medical device that received FDA 510(k) clearance on 2000-03-21. The listed applicant is Indus Medicare , Ltd.. The 510(k) number is K000039.

When did INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED receive FDA 510(k) clearance?

INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED received FDA 510(k) clearance on 2000-03-21, under 510(k) number K000039.

Who is the listed applicant for INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED?

The FDA 510(k) record lists Indus Medicare , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED?

The FDA product code for INVIGRA MALE LATEX CONDOM YELLOW COLORED AND BANANA FLAVORED is HIS.

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Other records listing Indus Medicare , Ltd. 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.

K022614INVIGRAK020223INVIGRAK000038INVIGRA MALE LATEX CONDOM GREEN COLORED AND MINT FLAVOREDK000040INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVOREDK993693INVIGRAK992438INVIGRA PLUS (WITH SPERMICIDAL LUBRICANT)

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Related Devices (Code: HIS)

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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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