MEDTRADE PRODUCTS CELOX SOLBAG, ANTI - COAGULANT
K-Number: K072328 · 2007-12-21
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Device Summary
Frequently Asked Questions
What is the MEDTRADE PRODUCTS CELOX SOLBAG, ANTI - COAGULANT?
MEDTRADE PRODUCTS CELOX SOLBAG, ANTI - COAGULANT is a medical device that received FDA 510(k) clearance on 2007-12-21. The listed applicant is Medtrade Products , Ltd.. The 510(k) number is K072328.
When did MEDTRADE PRODUCTS CELOX SOLBAG, ANTI - COAGULANT receive FDA 510(k) clearance?
MEDTRADE PRODUCTS CELOX SOLBAG, ANTI - COAGULANT received FDA 510(k) clearance on 2007-12-21, under 510(k) number K072328.
Who is the listed applicant for MEDTRADE PRODUCTS CELOX SOLBAG, ANTI - COAGULANT?
The FDA 510(k) record lists Medtrade Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDTRADE PRODUCTS CELOX SOLBAG, ANTI - COAGULANT?
The FDA product code for MEDTRADE PRODUCTS CELOX SOLBAG, ANTI - COAGULANT 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 Medtrade Products , 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: 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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