BIRTHTRACK
K-Number: K080672 · 2008-07-08
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Device Summary
Frequently Asked Questions
What is the BIRTHTRACK?
BIRTHTRACK is a medical device that received FDA 510(k) clearance on 2008-07-08. The listed applicant is Barnev, Ltd.. The 510(k) number is K080672.
When did BIRTHTRACK receive FDA 510(k) clearance?
BIRTHTRACK received FDA 510(k) clearance on 2008-07-08, under 510(k) number K080672.
Who is the listed applicant for BIRTHTRACK?
The FDA 510(k) record lists Barnev, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIRTHTRACK?
The FDA product code for BIRTHTRACK is NPB.
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 Barnev, Ltd. 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: NPB)
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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