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FDA 510(k)

FLEXIFO ENTERAL NUTRITION PUMP

K-Number: K791528 · 1979-09-12

ApplicantAbbott Laboratories
Decision Date1979-09-12
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLEXIFO ENTERAL NUTRITION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1979-09-12 under 510(k) number K791528. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIFO ENTERAL NUTRITION PUMP?

FLEXIFO ENTERAL NUTRITION PUMP is a medical device that received FDA 510(k) clearance on 1979-09-12. The listed applicant is Abbott Laboratories. The 510(k) number is K791528.

When did FLEXIFO ENTERAL NUTRITION PUMP receive FDA 510(k) clearance?

FLEXIFO ENTERAL NUTRITION PUMP received FDA 510(k) clearance on 1979-09-12, under 510(k) number K791528.

Who is the listed applicant for FLEXIFO ENTERAL NUTRITION PUMP?

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 FLEXIFO ENTERAL NUTRITION PUMP?

The FDA product code for FLEXIFO ENTERAL NUTRITION PUMP is FRN.

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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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