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FDA 510(k)

FLEXIFLO QUANTUM ENT. PUMP SETS AND ENT. NUT. CONT

K-Number: K915735 · 1992-06-24

ApplicantAbbott Laboratories
Decision Date1992-06-24
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLEXIFLO QUANTUM ENT. PUMP SETS AND ENT. NUT. CONT is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1992-06-24 under 510(k) number K915735. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIFLO QUANTUM ENT. PUMP SETS AND ENT. NUT. CONT?

FLEXIFLO QUANTUM ENT. PUMP SETS AND ENT. NUT. CONT is a medical device that received FDA 510(k) clearance on 1992-06-24. The listed applicant is Abbott Laboratories. The 510(k) number is K915735.

When did FLEXIFLO QUANTUM ENT. PUMP SETS AND ENT. NUT. CONT receive FDA 510(k) clearance?

FLEXIFLO QUANTUM ENT. PUMP SETS AND ENT. NUT. CONT received FDA 510(k) clearance on 1992-06-24, under 510(k) number K915735.

Who is the listed applicant for FLEXIFLO QUANTUM ENT. PUMP SETS AND ENT. NUT. CONT?

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 QUANTUM ENT. PUMP SETS AND ENT. NUT. CONT?

The FDA product code for FLEXIFLO QUANTUM ENT. PUMP SETS AND ENT. NUT. CONT is KNT.

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Related Devices (Code: KNT)

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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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