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FDA 510(k)

FLEXIFLO-III PORTABLE ENTERAL NUTRI

K-Number: K841784 · 1984-06-07

ApplicantAbbott Laboratories
Decision Date1984-06-07
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLEXIFLO-III PORTABLE ENTERAL NUTRI is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1984-06-07 under 510(k) number K841784. 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 FLEXIFLO-III PORTABLE ENTERAL NUTRI?

FLEXIFLO-III PORTABLE ENTERAL NUTRI is a medical device that received FDA 510(k) clearance on 1984-06-07. The listed applicant is Abbott Laboratories. The 510(k) number is K841784.

When did FLEXIFLO-III PORTABLE ENTERAL NUTRI receive FDA 510(k) clearance?

FLEXIFLO-III PORTABLE ENTERAL NUTRI received FDA 510(k) clearance on 1984-06-07, under 510(k) number K841784.

Who is the listed applicant for FLEXIFLO-III PORTABLE ENTERAL NUTRI?

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-III PORTABLE ENTERAL NUTRI?

The FDA product code for FLEXIFLO-III PORTABLE ENTERAL NUTRI 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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