ENTERNAL PUMP SET W/INTEGRAL CONTAINER
K-Number: K810996 · 1981-04-29
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Device Summary
Frequently Asked Questions
What is the ENTERNAL PUMP SET W/INTEGRAL CONTAINER?
ENTERNAL PUMP SET W/INTEGRAL CONTAINER is a medical device that received FDA 510(k) clearance on 1981-04-29. The listed applicant is Abbott Laboratories. The 510(k) number is K810996.
When did ENTERNAL PUMP SET W/INTEGRAL CONTAINER receive FDA 510(k) clearance?
ENTERNAL PUMP SET W/INTEGRAL CONTAINER received FDA 510(k) clearance on 1981-04-29, under 510(k) number K810996.
Who is the listed applicant for ENTERNAL PUMP SET W/INTEGRAL CONTAINER?
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 ENTERNAL PUMP SET W/INTEGRAL CONTAINER?
The FDA product code for ENTERNAL PUMP SET W/INTEGRAL CONTAINER is KNT.
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 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: KNT)
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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