V-2200 INFANT INCUBATOR
K-Number: K061280 · 2006-06-27
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Device Summary
Frequently Asked Questions
What is the V-2200 INFANT INCUBATOR?
V-2200 INFANT INCUBATOR is a medical device that received FDA 510(k) clearance on 2006-06-27. The listed applicant is Neoforce Group, Inc.. The 510(k) number is K061280.
When did V-2200 INFANT INCUBATOR receive FDA 510(k) clearance?
V-2200 INFANT INCUBATOR received FDA 510(k) clearance on 2006-06-27, under 510(k) number K061280.
Who is the listed applicant for V-2200 INFANT INCUBATOR?
The FDA 510(k) record lists Neoforce Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for V-2200 INFANT INCUBATOR?
The FDA product code for V-2200 INFANT INCUBATOR is FMZ.
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 Neoforce Group, 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: FMZ)
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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