FDA 510(k)

IPI DUAL LUMEN PORT

K-Number: K934167 · 1994-07-14

ApplicantPudenz-Schulte Medical Research Corp.

Decision Date1994-07-14

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

IPI DUAL LUMEN PORT is the device name listed in this FDA 510(k) record. The listed applicant is Pudenz-Schulte Medical Research Corp.. It received FDA 510(k) clearance on 1994-07-14 under 510(k) number K934167. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPI DUAL LUMEN PORT?

IPI DUAL LUMEN PORT is a medical device that received FDA 510(k) clearance on 1994-07-14. The listed applicant is Pudenz-Schulte Medical Research Corp.. The 510(k) number is K934167.

When did IPI DUAL LUMEN PORT receive FDA 510(k) clearance?

IPI DUAL LUMEN PORT received FDA 510(k) clearance on 1994-07-14, under 510(k) number K934167.

Who is the listed applicant for IPI DUAL LUMEN PORT?

The FDA 510(k) record lists Pudenz-Schulte Medical Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IPI DUAL LUMEN PORT?

The FDA product code for IPI DUAL LUMEN PORT is LJT.

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Related Devices (Code: LJT)

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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.