SOFTSEAL-C
K-Number: K112864 · 2012-08-02
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Device Summary
Frequently Asked Questions
What is the SOFTSEAL-C?
SOFTSEAL-C is a medical device that received FDA 510(k) clearance on 2012-08-02. The listed applicant is Chitogen, Inc.. The 510(k) number is K112864.
When did SOFTSEAL-C receive FDA 510(k) clearance?
SOFTSEAL-C received FDA 510(k) clearance on 2012-08-02, under 510(k) number K112864.
Who is the listed applicant for SOFTSEAL-C?
The FDA 510(k) record lists Chitogen, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOFTSEAL-C?
The FDA product code for SOFTSEAL-C is QSY.
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 Chitogen, 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: QSY)
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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