TOTAL BILIRUBIN L.F.
K-Number: K895822 · 1989-11-14
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Device Summary
Frequently Asked Questions
What is the TOTAL BILIRUBIN L.F.?
TOTAL BILIRUBIN L.F. is a medical device that received FDA 510(k) clearance on 1989-11-14. The listed applicant is Sclavo, Inc.. The 510(k) number is K895822.
When did TOTAL BILIRUBIN L.F. receive FDA 510(k) clearance?
TOTAL BILIRUBIN L.F. received FDA 510(k) clearance on 1989-11-14, under 510(k) number K895822.
Who is the listed applicant for TOTAL BILIRUBIN L.F.?
The FDA 510(k) record lists Sclavo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TOTAL BILIRUBIN L.F.?
The FDA product code for TOTAL BILIRUBIN L.F. is CIG.
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 Sclavo, 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: CIG)
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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