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FDA 510(k)

ETHOX RELIA-FLO 2001 ENTERAL FEED

K-Number: K841512 · 1984-05-21

ApplicantEthox Corp.
Decision Date1984-05-21
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ETHOX RELIA-FLO 2001 ENTERAL FEED is the device name listed in this FDA 510(k) record. The listed applicant is Ethox Corp.. It received FDA 510(k) clearance on 1984-05-21 under 510(k) number K841512. 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 ETHOX RELIA-FLO 2001 ENTERAL FEED?

ETHOX RELIA-FLO 2001 ENTERAL FEED is a medical device that received FDA 510(k) clearance on 1984-05-21. The listed applicant is Ethox Corp.. The 510(k) number is K841512.

When did ETHOX RELIA-FLO 2001 ENTERAL FEED receive FDA 510(k) clearance?

ETHOX RELIA-FLO 2001 ENTERAL FEED received FDA 510(k) clearance on 1984-05-21, under 510(k) number K841512.

Who is the listed applicant for ETHOX RELIA-FLO 2001 ENTERAL FEED?

The FDA 510(k) record lists Ethox Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ETHOX RELIA-FLO 2001 ENTERAL FEED?

The FDA product code for ETHOX RELIA-FLO 2001 ENTERAL FEED is FRN.

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Other records listing Ethox Corp. as applicant

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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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