KNIGHT LIGHT NONLUBRICATED CONDOM
K-Number: K960552 · 1997-11-20
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Device Summary
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.
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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