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FDA 510(k)

RHYDER DIAGNOSTIC CATHETER

K-Number: K962307 · 1996-09-17

ApplicantFidus Medical Technology Corp.
Decision Date1996-09-17
Product CodeDRF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RHYDER DIAGNOSTIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Fidus Medical Technology Corp.. It received FDA 510(k) clearance on 1996-09-17 under 510(k) number K962307. 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 RHYDER DIAGNOSTIC CATHETER?

RHYDER DIAGNOSTIC CATHETER is a medical device that received FDA 510(k) clearance on 1996-09-17. The listed applicant is Fidus Medical Technology Corp.. The 510(k) number is K962307.

When did RHYDER DIAGNOSTIC CATHETER receive FDA 510(k) clearance?

RHYDER DIAGNOSTIC CATHETER received FDA 510(k) clearance on 1996-09-17, under 510(k) number K962307.

Who is the listed applicant for RHYDER DIAGNOSTIC CATHETER?

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

What is the FDA product code for RHYDER DIAGNOSTIC CATHETER?

The FDA product code for RHYDER DIAGNOSTIC CATHETER is DRF.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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