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FDA 510(k)

DAIG ELECTROPHYSIOLOGY CATHETER W/INFUSION LUMEN

K-Number: K914278 · 1992-03-04

ApplicantDaig Corp.
Decision Date1992-03-04
Product CodeDRF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DAIG ELECTROPHYSIOLOGY CATHETER W/INFUSION LUMEN is the device name listed in this FDA 510(k) record. The listed applicant is Daig Corp.. It received FDA 510(k) clearance on 1992-03-04 under 510(k) number K914278. The device is classified under product code DRF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAIG ELECTROPHYSIOLOGY CATHETER W/INFUSION LUMEN?

DAIG ELECTROPHYSIOLOGY CATHETER W/INFUSION LUMEN is a medical device that received FDA 510(k) clearance on 1992-03-04. The listed applicant is Daig Corp.. The 510(k) number is K914278.

When did DAIG ELECTROPHYSIOLOGY CATHETER W/INFUSION LUMEN receive FDA 510(k) clearance?

DAIG ELECTROPHYSIOLOGY CATHETER W/INFUSION LUMEN received FDA 510(k) clearance on 1992-03-04, under 510(k) number K914278.

Who is the listed applicant for DAIG ELECTROPHYSIOLOGY CATHETER W/INFUSION LUMEN?

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

What is the FDA product code for DAIG ELECTROPHYSIOLOGY CATHETER W/INFUSION LUMEN?

The FDA product code for DAIG ELECTROPHYSIOLOGY CATHETER W/INFUSION LUMEN is DRF.

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Related Devices (Code: DRF)

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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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