FREEALGIN
K-Number: K070700 · 2007-04-25
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Device Summary
Frequently Asked Questions
What is the FREEALGIN?
FREEALGIN is a medical device that received FDA 510(k) clearance on 2007-04-25. The listed applicant is Zhermack S.P.A.. The 510(k) number is K070700.
When did FREEALGIN receive FDA 510(k) clearance?
FREEALGIN received FDA 510(k) clearance on 2007-04-25, under 510(k) number K070700.
Who is the listed applicant for FREEALGIN?
The FDA 510(k) record lists Zhermack S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FREEALGIN?
The FDA product code for FREEALGIN is ELW.
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 Zhermack S.P.A. 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: ELW)
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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