TBIL
K-Number: K983133 · 1998-09-16
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Device Summary
Frequently Asked Questions
What is the TBIL?
TBIL is a medical device that received FDA 510(k) clearance on 1998-09-16. The listed applicant is Abbott Laboratories. The 510(k) number is K983133.
When did TBIL receive FDA 510(k) clearance?
TBIL received FDA 510(k) clearance on 1998-09-16, under 510(k) number K983133.
Who is the listed applicant for TBIL?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TBIL?
The FDA product code for TBIL is CIG.
Other records listing Abbott Laboratories 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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