MISTY OX TURBOHEATER
K-Number: K962438 · 1997-01-13
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Device Summary
Frequently Asked Questions
What is the MISTY OX TURBOHEATER?
MISTY OX TURBOHEATER is a medical device that received FDA 510(k) clearance on 1997-01-13. The listed applicant is Vital Signs, Inc.. The 510(k) number is K962438.
When did MISTY OX TURBOHEATER receive FDA 510(k) clearance?
MISTY OX TURBOHEATER received FDA 510(k) clearance on 1997-01-13, under 510(k) number K962438.
Who is the listed applicant for MISTY OX TURBOHEATER?
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 MISTY OX TURBOHEATER?
The FDA product code for MISTY OX TURBOHEATER is CAF.
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: CAF)
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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