SAFESKIN SUPRA
K-Number: K953015 · 1995-08-28
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Device Summary
Frequently Asked Questions
What is the SAFESKIN SUPRA?
SAFESKIN SUPRA is a medical device that received FDA 510(k) clearance on 1995-08-28. The listed applicant is Safeskin Corp.. The 510(k) number is K953015.
When did SAFESKIN SUPRA receive FDA 510(k) clearance?
SAFESKIN SUPRA received FDA 510(k) clearance on 1995-08-28, under 510(k) number K953015.
Who is the listed applicant for SAFESKIN SUPRA?
The FDA 510(k) record lists Safeskin Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SAFESKIN SUPRA?
The FDA product code for SAFESKIN SUPRA is KGO.
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 Safeskin 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: KGO)
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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