HOTLINE FLUID WARMER
K-Number: K911383 · 1991-10-17
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Device Summary
Frequently Asked Questions
What is the HOTLINE FLUID WARMER?
HOTLINE FLUID WARMER is a medical device that received FDA 510(k) clearance on 1991-10-17. The listed applicant is Level 1 Technologies, Inc.. The 510(k) number is K911383.
When did HOTLINE FLUID WARMER receive FDA 510(k) clearance?
HOTLINE FLUID WARMER received FDA 510(k) clearance on 1991-10-17, under 510(k) number K911383.
Who is the listed applicant for HOTLINE FLUID WARMER?
The FDA 510(k) record lists Level 1 Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HOTLINE FLUID WARMER?
The FDA product code for HOTLINE FLUID WARMER 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 Level 1 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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