FDA 510(k)

REDO CENTRAL VENOUS CATHETER-NEONATE

K-Number: K841443 · 1984-07-27

Decision Date1984-07-27

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

REDO CENTRAL VENOUS CATHETER-NEONATE is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Hospital Products, Inc.. It received FDA 510(k) clearance on 1984-07-27 under 510(k) number K841443. 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 REDO CENTRAL VENOUS CATHETER-NEONATE?

REDO CENTRAL VENOUS CATHETER-NEONATE is a medical device that received FDA 510(k) clearance on 1984-07-27. The listed applicant is Intl. Hospital Products, Inc.. The 510(k) number is K841443.

When did REDO CENTRAL VENOUS CATHETER-NEONATE receive FDA 510(k) clearance?

REDO CENTRAL VENOUS CATHETER-NEONATE received FDA 510(k) clearance on 1984-07-27, under 510(k) number K841443.

Who is the listed applicant for REDO CENTRAL VENOUS CATHETER-NEONATE?

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

What is the FDA product code for REDO CENTRAL VENOUS CATHETER-NEONATE?

The FDA product code for REDO CENTRAL VENOUS CATHETER-NEONATE is LJS.

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Other records listing Intl. Hospital Products, Inc. as applicant

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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.