ALGICELL AG
K-Number: K052536 · 2006-09-13
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Device Summary
Frequently Asked Questions
What is the ALGICELL AG?
ALGICELL AG is a medical device that received FDA 510(k) clearance on 2006-09-13. The listed applicant is Derma Sciences Canada, Inc.. The 510(k) number is K052536.
When did ALGICELL AG receive FDA 510(k) clearance?
ALGICELL AG received FDA 510(k) clearance on 2006-09-13, under 510(k) number K052536.
Who is the listed applicant for ALGICELL AG?
The FDA 510(k) record lists Derma Sciences Canada, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALGICELL AG?
The FDA product code for ALGICELL AG is FRO. This falls under the Anesthesiology category.
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 Derma Sciences Canada, Inc. 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: FRO)
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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