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FDA 510(k)

3F AND 4F IRRIGATION EMBOLECTOMY CATHETERS

K-Number: K897184 · 1990-03-14

ApplicantCathlab Corp.
Decision Date1990-03-14
Product CodeDXE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

3F AND 4F IRRIGATION EMBOLECTOMY CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Cathlab Corp.. It received FDA 510(k) clearance on 1990-03-14 under 510(k) number K897184. The device is classified under product code DXE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3F AND 4F IRRIGATION EMBOLECTOMY CATHETERS?

3F AND 4F IRRIGATION EMBOLECTOMY CATHETERS is a medical device that received FDA 510(k) clearance on 1990-03-14. The listed applicant is Cathlab Corp.. The 510(k) number is K897184.

When did 3F AND 4F IRRIGATION EMBOLECTOMY CATHETERS receive FDA 510(k) clearance?

3F AND 4F IRRIGATION EMBOLECTOMY CATHETERS received FDA 510(k) clearance on 1990-03-14, under 510(k) number K897184.

Who is the listed applicant for 3F AND 4F IRRIGATION EMBOLECTOMY CATHETERS?

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

What is the FDA product code for 3F AND 4F IRRIGATION EMBOLECTOMY CATHETERS?

The FDA product code for 3F AND 4F IRRIGATION EMBOLECTOMY CATHETERS is DXE.

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Other records listing Cathlab Corp. as applicant

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.

K910917CATHLAB SILICONE BILIARY BALLOON CATHETERK910916CATHLAB SILICONE OCCLUSION BALLOON CATHETERK905139CATHLAB SILICONE ARTERIAL EMBOLECTOMY CATHETERK897051MILLER PERCUTANEOUS ANGIOGRAPHIC/SCOPIC IRRI. CATHK893435SILICONE FLOW-DIRECTED THERMODILUTION CATHETERK893680SILICONE BI-LUMEN IRRIGATION EMBOLECTOMY CATH.

View all 8 devices →

Related Devices (Code: DXE)

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.

K240078Fogarty Thru-Lumen Embolectomy CatheterEdwards Lifesciences, LLCK241330Fogarty Fortis Arterial Embolectomy CatheterEdwards LifesciencesK233820Fogarty Arterial Embolectomy Catheter with Gate ValveEdwards LifesciencesK233819Fogarty Venous Thrombectomy CathetersEdwards Lifesciences, LLCK233619Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy CathetersEdwards LifesciencesK213771Merlin Aspiration SystemMivi Neurovascular, 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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