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FDA 510(k)

DAIG ELECTROPHYSIOLOGY CATHETER

K-Number: K894500 · 1989-09-18

ApplicantDaig Corp.
Decision Date1989-09-18
Product CodeDRF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DAIG ELECTROPHYSIOLOGY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Daig Corp.. It received FDA 510(k) clearance on 1989-09-18 under 510(k) number K894500. 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?

DAIG ELECTROPHYSIOLOGY CATHETER is a medical device that received FDA 510(k) clearance on 1989-09-18. The listed applicant is Daig Corp.. The 510(k) number is K894500.

When did DAIG ELECTROPHYSIOLOGY CATHETER receive FDA 510(k) clearance?

DAIG ELECTROPHYSIOLOGY CATHETER received FDA 510(k) clearance on 1989-09-18, under 510(k) number K894500.

Who is the listed applicant for DAIG ELECTROPHYSIOLOGY CATHETER?

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?

The FDA product code for DAIG ELECTROPHYSIOLOGY CATHETER is DRF.

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Other records listing Daig Corp. as applicant

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Related Devices (Code: DRF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252794Vision-MR™ Diagnostic CatheterImricor Medical Systems, Inc.K250590MAGiC Sweep™ EP Mapping CatheterStereotaxis, Inc.K250310VIKING™ Fixed Curve Diagnostic CatheterBoston Scientific CorporationK240366EP•XT™ Unidirectional Steerable Diagnostic Catheter; Dynamic Tip™ Unidirectional Steerable Diagnostic Catheter; Dynamic XT™ Unidirectional Steerable Diagnostic CatheterBoston Scientific CorporationK233900Nordica PV Cryo Mapping CatheterSynaptic Medical CorporationK233397Cosine-10TM Diagnostic CatheterMedtronic, Inc.

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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