TIANJIN MEDIS DISPOSABLE INFUSION SET
K-Number: K060082 · 2006-03-31
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Device Summary
Frequently Asked Questions
What is the TIANJIN MEDIS DISPOSABLE INFUSION SET?
TIANJIN MEDIS DISPOSABLE INFUSION SET is a medical device that received FDA 510(k) clearance on 2006-03-31. The listed applicant is Tianjin Medis International Trade Co., Ltd.. The 510(k) number is K060082.
When did TIANJIN MEDIS DISPOSABLE INFUSION SET receive FDA 510(k) clearance?
TIANJIN MEDIS DISPOSABLE INFUSION SET received FDA 510(k) clearance on 2006-03-31, under 510(k) number K060082.
Who is the listed applicant for TIANJIN MEDIS DISPOSABLE INFUSION SET?
The FDA 510(k) record lists Tianjin Medis International Trade Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TIANJIN MEDIS DISPOSABLE INFUSION SET?
The FDA product code for TIANJIN MEDIS DISPOSABLE INFUSION SET is FPA.
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: FPA)
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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