ENFLOW IV FLUID WARMER
K-Number: K112902 · 2012-03-14
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Device Summary
Frequently Asked Questions
What is the ENFLOW IV FLUID WARMER?
ENFLOW IV FLUID WARMER is a medical device that received FDA 510(k) clearance on 2012-03-14. The listed applicant is Vital Signs, Inc.. The 510(k) number is K112902.
When did ENFLOW IV FLUID WARMER receive FDA 510(k) clearance?
ENFLOW IV FLUID WARMER received FDA 510(k) clearance on 2012-03-14, under 510(k) number K112902.
Who is the listed applicant for ENFLOW IV FLUID WARMER?
The FDA 510(k) record lists Vital Signs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENFLOW IV FLUID WARMER?
The FDA product code for ENFLOW IV 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 Vital Signs, 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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