UNICRYL M
K-Number: K042285 · 2004-12-10
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Device Summary
Frequently Asked Questions
What is the UNICRYL M?
UNICRYL M is a medical device that received FDA 510(k) clearance on 2004-12-10. The listed applicant is United Medical Industries Co. , Ltd.. The 510(k) number is K042285.
When did UNICRYL M receive FDA 510(k) clearance?
UNICRYL M received FDA 510(k) clearance on 2004-12-10, under 510(k) number K042285.
Who is the listed applicant for UNICRYL M?
The FDA 510(k) record lists United Medical Industries Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNICRYL M?
The FDA product code for UNICRYL M is NEW.
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 United Medical Industries Co. , 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: NEW)
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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