CODE BLUE MANUAL RESUSCITATOR
K-Number: K831885 · 1983-09-08
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Device Summary
Frequently Asked Questions
What is the CODE BLUE MANUAL RESUSCITATOR?
CODE BLUE MANUAL RESUSCITATOR is a medical device that received FDA 510(k) clearance on 1983-09-08. The listed applicant is Vital Signs, Inc.. The 510(k) number is K831885.
When did CODE BLUE MANUAL RESUSCITATOR receive FDA 510(k) clearance?
CODE BLUE MANUAL RESUSCITATOR received FDA 510(k) clearance on 1983-09-08, under 510(k) number K831885.
Who is the listed applicant for CODE BLUE 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 CODE BLUE MANUAL RESUSCITATOR?
The FDA product code for CODE BLUE 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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