THE BELMONT BUDDY LITE FLUID WARMER
K-Number: K112639 · 2011-11-16
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Device Summary
Frequently Asked Questions
What is the THE BELMONT BUDDY LITE FLUID WARMER?
THE BELMONT BUDDY LITE FLUID WARMER is a medical device that received FDA 510(k) clearance on 2011-11-16. The listed applicant is Belmont Instrument Corp.. The 510(k) number is K112639.
When did THE BELMONT BUDDY LITE FLUID WARMER receive FDA 510(k) clearance?
THE BELMONT BUDDY LITE FLUID WARMER received FDA 510(k) clearance on 2011-11-16, under 510(k) number K112639.
Who is the listed applicant for THE BELMONT BUDDY LITE FLUID WARMER?
The FDA 510(k) record lists Belmont Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THE BELMONT BUDDY LITE FLUID WARMER?
The FDA product code for THE BELMONT BUDDY LITE 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 Belmont Instrument 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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