BARO/TRAC II & VITA/TRAC, VITAL SIGN MON
K-Number: K801389 · 1980-07-28
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Device Summary
Frequently Asked Questions
What is the BARO/TRAC II & VITA/TRAC, VITAL SIGN MON?
BARO/TRAC II & VITA/TRAC, VITAL SIGN MON is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Bib, Inc.. The 510(k) number is K801389.
When did BARO/TRAC II & VITA/TRAC, VITAL SIGN MON receive FDA 510(k) clearance?
BARO/TRAC II & VITA/TRAC, VITAL SIGN MON received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801389.
Who is the listed applicant for BARO/TRAC II & VITA/TRAC, VITAL SIGN MON?
The FDA 510(k) record lists Bib, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BARO/TRAC II & VITA/TRAC, VITAL SIGN MON?
The FDA product code for BARO/TRAC II & VITA/TRAC, VITAL SIGN MON is DXN.
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 Bib, 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: DXN)
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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