THERMACYL BLOOD/FLUID WARMER
K-Number: K953741 · 1996-06-26
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Device Summary
Frequently Asked Questions
What is the THERMACYL BLOOD/FLUID WARMER?
THERMACYL BLOOD/FLUID WARMER is a medical device that received FDA 510(k) clearance on 1996-06-26. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K953741.
When did THERMACYL BLOOD/FLUID WARMER receive FDA 510(k) clearance?
THERMACYL BLOOD/FLUID WARMER received FDA 510(k) clearance on 1996-06-26, under 510(k) number K953741.
Who is the listed applicant for THERMACYL BLOOD/FLUID WARMER?
The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THERMACYL BLOOD/FLUID WARMER?
The FDA product code for THERMACYL BLOOD/FLUID WARMER is BSB.
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 Baxter Healthcare Corp 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: BSB)
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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