FDA 510(k)

GRECO-HARVEY SURFACT BOND CATH HYPERALIMENTATION

K-Number: K851243 · 1986-03-14

Decision Date1986-03-14

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

GRECO-HARVEY SURFACT BOND CATH HYPERALIMENTATION is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 1986-03-14 under 510(k) number K851243. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRECO-HARVEY SURFACT BOND CATH HYPERALIMENTATION?

GRECO-HARVEY SURFACT BOND CATH HYPERALIMENTATION is a medical device that received FDA 510(k) clearance on 1986-03-14. The listed applicant is Cook, Inc.. The 510(k) number is K851243.

When did GRECO-HARVEY SURFACT BOND CATH HYPERALIMENTATION receive FDA 510(k) clearance?

GRECO-HARVEY SURFACT BOND CATH HYPERALIMENTATION received FDA 510(k) clearance on 1986-03-14, under 510(k) number K851243.

Who is the listed applicant for GRECO-HARVEY SURFACT BOND CATH HYPERALIMENTATION?

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

What is the FDA product code for GRECO-HARVEY SURFACT BOND CATH HYPERALIMENTATION?

The FDA product code for GRECO-HARVEY SURFACT BOND CATH HYPERALIMENTATION is LJS.

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Related Devices (Code: LJS)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.