STAT BLUE DISPOS. MANUAL RESUSCITATOR
K-Number: K850436 · 1985-02-26
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Device Summary
Frequently Asked Questions
What is the STAT BLUE DISPOS. MANUAL RESUSCITATOR?
STAT BLUE DISPOS. MANUAL RESUSCITATOR is a medical device that received FDA 510(k) clearance on 1985-02-26. The listed applicant is Vital Signs, Inc.. The 510(k) number is K850436.
When did STAT BLUE DISPOS. MANUAL RESUSCITATOR receive FDA 510(k) clearance?
STAT BLUE DISPOS. MANUAL RESUSCITATOR received FDA 510(k) clearance on 1985-02-26, under 510(k) number K850436.
Who is the listed applicant for STAT BLUE DISPOS. MANUAL RESUSCITATOR?
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 STAT BLUE DISPOS. MANUAL RESUSCITATOR?
The FDA product code for STAT BLUE DISPOS. MANUAL RESUSCITATOR is BTM.
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: BTM)
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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