FLEXIFLO COMPANION ENTERAL PUMP SETS AND CONTAINER
K-Number: K921697 · 1992-08-25
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Device Summary
Frequently Asked Questions
What is the FLEXIFLO COMPANION ENTERAL PUMP SETS AND CONTAINER?
FLEXIFLO COMPANION ENTERAL PUMP SETS AND CONTAINER is a medical device that received FDA 510(k) clearance on 1992-08-25. The listed applicant is Abbott Laboratories. The 510(k) number is K921697.
When did FLEXIFLO COMPANION ENTERAL PUMP SETS AND CONTAINER receive FDA 510(k) clearance?
FLEXIFLO COMPANION ENTERAL PUMP SETS AND CONTAINER received FDA 510(k) clearance on 1992-08-25, under 510(k) number K921697.
Who is the listed applicant for FLEXIFLO COMPANION ENTERAL PUMP SETS AND 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 FLEXIFLO COMPANION ENTERAL PUMP SETS AND CONTAINER?
The FDA product code for FLEXIFLO COMPANION ENTERAL PUMP SETS AND 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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