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FDA 510(k)

AVD INTIMAX OCCLUSION CATHETER

K-Number: K910339 · 1991-05-29

ApplicantApplied Vascular Devices, Inc.
Decision Date1991-05-29
Product CodeDQT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AVD INTIMAX OCCLUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Applied Vascular Devices, Inc.. It received FDA 510(k) clearance on 1991-05-29 under 510(k) number K910339. The device is classified under product code DQT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AVD INTIMAX OCCLUSION CATHETER?

AVD INTIMAX OCCLUSION CATHETER is a medical device that received FDA 510(k) clearance on 1991-05-29. The listed applicant is Applied Vascular Devices, Inc.. The 510(k) number is K910339.

When did AVD INTIMAX OCCLUSION CATHETER receive FDA 510(k) clearance?

AVD INTIMAX OCCLUSION CATHETER received FDA 510(k) clearance on 1991-05-29, under 510(k) number K910339.

Who is the listed applicant for AVD INTIMAX OCCLUSION CATHETER?

The FDA 510(k) record lists Applied Vascular Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AVD INTIMAX OCCLUSION CATHETER?

The FDA product code for AVD INTIMAX OCCLUSION CATHETER is DQT.

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Other records listing Applied Vascular Devices, Inc. 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.

K911730SURGICAL OBTURATOR WITH SEALK911589DISPOSABLE SURGICAL TROCAR WITH SEALK910372INTIMAX THROMBECTOMY CATHETERK911181INTIMAX(TM) IRRIGATION CATHETERK910493AVD INTIMAX CHOLANGIOGRAPHY CATHETERK903848DIAGNOSTIC INTRASCULAR CATHETER

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Related Devices (Code: DQT)

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.

K983927GT1 FLOPPY, GT1 HI-PER FLEX, GT1 LIGHT SUPPORTArterial Vascular Engineering, Inc.K945963THE OMNIGUIDE GUIDING CATHETER WITH BALLOONMicro Interventional Systems, Inc.K910916CATHLAB SILICONE OCCLUSION BALLOON CATHETERCathlab Corp.K880860CORONARY OSTIUM OCCLUDER, CATALOG CODE 32015Dlp, Inc.K880231MODIFIED PRUITT IRRIGATION & OCCLUSION CATHETERIdeas For Medicine, Inc.K872090THE ROBICSEK - PRUITT AORTIC BALLOON OCCLUSION KITIdeas For Medicine, 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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