BISICO IMPRESSION SILICONES & ALGINATES
K-Number: K072577 · 2007-12-05
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Device Summary
Frequently Asked Questions
What is the BISICO IMPRESSION SILICONES & ALGINATES?
BISICO IMPRESSION SILICONES & ALGINATES is a medical device that received FDA 510(k) clearance on 2007-12-05. The listed applicant is Bisico GmbH & CO KG. The 510(k) number is K072577.
When did BISICO IMPRESSION SILICONES & ALGINATES receive FDA 510(k) clearance?
BISICO IMPRESSION SILICONES & ALGINATES received FDA 510(k) clearance on 2007-12-05, under 510(k) number K072577.
Who is the listed applicant for BISICO IMPRESSION SILICONES & ALGINATES?
The FDA 510(k) record lists Bisico GmbH & CO KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BISICO IMPRESSION SILICONES & ALGINATES?
The FDA product code for BISICO IMPRESSION SILICONES & ALGINATES 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.
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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