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FDA 510(k)

KNIGHT LIGHT NONLUBRICATED CONDOM

K-Number: K960552 · 1997-11-20

Decision Date1997-11-20
Product CodeHIS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KNIGHT LIGHT NONLUBRICATED CONDOM is the device name listed in this FDA 510(k) record. The listed applicant is Global Protection Corp.. It received FDA 510(k) clearance on 1997-11-20 under 510(k) number K960552. 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 KNIGHT LIGHT NONLUBRICATED CONDOM?

KNIGHT LIGHT NONLUBRICATED CONDOM is a medical device that received FDA 510(k) clearance on 1997-11-20. The listed applicant is Global Protection Corp.. The 510(k) number is K960552.

When did KNIGHT LIGHT NONLUBRICATED CONDOM receive FDA 510(k) clearance?

KNIGHT LIGHT NONLUBRICATED CONDOM received FDA 510(k) clearance on 1997-11-20, under 510(k) number K960552.

Who is the listed applicant for KNIGHT LIGHT NONLUBRICATED CONDOM?

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

What is the FDA product code for KNIGHT LIGHT NONLUBRICATED CONDOM?

The FDA product code for KNIGHT LIGHT NONLUBRICATED 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.

Other records listing Global Protection Corp. 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.

View all 10 devices →

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

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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