SAUFLON MULTIPURPOSE SOLUTION
K-Number: K130734 · 2013-05-15
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Device Summary
Frequently Asked Questions
What is the SAUFLON MULTIPURPOSE SOLUTION?
SAUFLON MULTIPURPOSE SOLUTION is a medical device that received FDA 510(k) clearance on 2013-05-15. The listed applicant is Sauflon Pharmaceuticals, Ltd.. The 510(k) number is K130734.
When did SAUFLON MULTIPURPOSE SOLUTION receive FDA 510(k) clearance?
SAUFLON MULTIPURPOSE SOLUTION received FDA 510(k) clearance on 2013-05-15, under 510(k) number K130734.
Who is the listed applicant for SAUFLON MULTIPURPOSE SOLUTION?
The FDA 510(k) record lists Sauflon Pharmaceuticals, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SAUFLON MULTIPURPOSE SOLUTION?
The FDA product code for SAUFLON MULTIPURPOSE SOLUTION is LPN.
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 Sauflon Pharmaceuticals, 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: LPN)
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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