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FDA 510(k)

LOVESAFE CONTRACEPTIVE CONDOMS, TYPE NL-50

K-Number: K863706 · 1986-09-26

Decision Date1986-09-26
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LOVESAFE CONTRACEPTIVE CONDOMS, TYPE NL-50 is the device name listed in this FDA 510(k) record. The listed applicant is Manexim Multicorp, Ltd.. It received FDA 510(k) clearance on 1986-09-26 under 510(k) number K863706. 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 LOVESAFE CONTRACEPTIVE CONDOMS, TYPE NL-50?

LOVESAFE CONTRACEPTIVE CONDOMS, TYPE NL-50 is a medical device that received FDA 510(k) clearance on 1986-09-26. The listed applicant is Manexim Multicorp, Ltd.. The 510(k) number is K863706.

When did LOVESAFE CONTRACEPTIVE CONDOMS, TYPE NL-50 receive FDA 510(k) clearance?

LOVESAFE CONTRACEPTIVE CONDOMS, TYPE NL-50 received FDA 510(k) clearance on 1986-09-26, under 510(k) number K863706.

Who is the listed applicant for LOVESAFE CONTRACEPTIVE CONDOMS, TYPE NL-50?

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

What is the FDA product code for LOVESAFE CONTRACEPTIVE CONDOMS, TYPE NL-50?

The FDA product code for LOVESAFE CONTRACEPTIVE CONDOMS, TYPE NL-50 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 Manexim Multicorp, 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.

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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