MAXONE IV FLUID/BLOOD WARMER, MODEL 102
K-Number: K023653 · 2003-01-17
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Device Summary
Frequently Asked Questions
What is the MAXONE IV FLUID/BLOOD WARMER, MODEL 102?
MAXONE IV FLUID/BLOOD WARMER, MODEL 102 is a medical device that received FDA 510(k) clearance on 2003-01-17. The listed applicant is Automatic Medical Technologies, Inc.. The 510(k) number is K023653.
When did MAXONE IV FLUID/BLOOD WARMER, MODEL 102 receive FDA 510(k) clearance?
MAXONE IV FLUID/BLOOD WARMER, MODEL 102 received FDA 510(k) clearance on 2003-01-17, under 510(k) number K023653.
Who is the listed applicant for MAXONE IV FLUID/BLOOD WARMER, MODEL 102?
The FDA 510(k) record lists Automatic Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAXONE IV FLUID/BLOOD WARMER, MODEL 102?
The FDA product code for MAXONE IV FLUID/BLOOD WARMER, MODEL 102 is LGZ.
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 Automatic Medical Technologies, 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: LGZ)
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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