PEDIATRIC BELLOWS
K-Number: K864431 · 1987-01-12
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Device Summary
Frequently Asked Questions
What is the PEDIATRIC BELLOWS?
PEDIATRIC BELLOWS is a medical device that received FDA 510(k) clearance on 1987-01-12. The listed applicant is Draeger Medical, Inc.. The 510(k) number is K864431.
When did PEDIATRIC BELLOWS receive FDA 510(k) clearance?
PEDIATRIC BELLOWS received FDA 510(k) clearance on 1987-01-12, under 510(k) number K864431.
Who is the listed applicant for PEDIATRIC BELLOWS?
The FDA 510(k) record lists Draeger Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PEDIATRIC BELLOWS?
The FDA product code for PEDIATRIC BELLOWS is CBK.
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 Draeger Medical, 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: CBK)
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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