ISOLETTE INFANT INCUBATOR
K-Number: K960980 · 1996-07-30
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Device Summary
Frequently Asked Questions
What is the ISOLETTE INFANT INCUBATOR?
ISOLETTE INFANT INCUBATOR is a medical device that received FDA 510(k) clearance on 1996-07-30. The listed applicant is Air-Shields, Inc.. The 510(k) number is K960980.
When did ISOLETTE INFANT INCUBATOR receive FDA 510(k) clearance?
ISOLETTE INFANT INCUBATOR received FDA 510(k) clearance on 1996-07-30, under 510(k) number K960980.
Who is the listed applicant for ISOLETTE INFANT INCUBATOR?
The FDA 510(k) record lists Air-Shields, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ISOLETTE INFANT INCUBATOR?
The FDA product code for ISOLETTE 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 Air-Shields, 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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