NBIL
K-Number: K983134 · 1998-09-23
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Device Summary
Frequently Asked Questions
What is the NBIL?
NBIL is a medical device that received FDA 510(k) clearance on 1998-09-23. The listed applicant is Abbott Laboratories. The 510(k) number is K983134.
When did NBIL receive FDA 510(k) clearance?
NBIL received FDA 510(k) clearance on 1998-09-23, under 510(k) number K983134.
Who is the listed applicant for NBIL?
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 NBIL?
The FDA product code for NBIL is MQM.
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: MQM)
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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