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FDA 510(k)

LOVIEL CONDOM

K-Number: K872861 · 1987-12-11

ApplicantLloviel Marketing Corp.
Decision Date1987-12-11
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LOVIEL CONDOM is the device name listed in this FDA 510(k) record. The listed applicant is Lloviel Marketing Corp.. It received FDA 510(k) clearance on 1987-12-11 under 510(k) number K872861. 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 LOVIEL CONDOM?

LOVIEL CONDOM is a medical device that received FDA 510(k) clearance on 1987-12-11. The listed applicant is Lloviel Marketing Corp.. The 510(k) number is K872861.

When did LOVIEL CONDOM receive FDA 510(k) clearance?

LOVIEL CONDOM received FDA 510(k) clearance on 1987-12-11, under 510(k) number K872861.

Who is the listed applicant for LOVIEL CONDOM?

The FDA 510(k) record lists Lloviel Marketing Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOVIEL CONDOM?

The FDA product code for LOVIEL CONDOM 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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