FDA 510(k)

ARROW-GEISS PERCUTANEOUS TPN KIT

K-Number: K844080 · 1985-04-17

Decision Date1985-04-17

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

ARROW-GEISS PERCUTANEOUS TPN KIT is the device name listed in this FDA 510(k) record. The listed applicant is Arrow Intl., Inc.. It received FDA 510(k) clearance on 1985-04-17 under 510(k) number K844080. 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 ARROW-GEISS PERCUTANEOUS TPN KIT?

ARROW-GEISS PERCUTANEOUS TPN KIT is a medical device that received FDA 510(k) clearance on 1985-04-17. The listed applicant is Arrow Intl., Inc.. The 510(k) number is K844080.

When did ARROW-GEISS PERCUTANEOUS TPN KIT receive FDA 510(k) clearance?

ARROW-GEISS PERCUTANEOUS TPN KIT received FDA 510(k) clearance on 1985-04-17, under 510(k) number K844080.

Who is the listed applicant for ARROW-GEISS PERCUTANEOUS TPN KIT?

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

What is the FDA product code for ARROW-GEISS PERCUTANEOUS TPN KIT?

The FDA product code for ARROW-GEISS PERCUTANEOUS TPN KIT 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.