Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PTA AND PTV

K-Number: K022722 · 2002-09-13

ApplicantNuMED, Inc.
Decision Date2002-09-13
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PTA AND PTV is the device name listed in this FDA 510(k) record. The listed applicant is NuMED, Inc.. It received FDA 510(k) clearance on 2002-09-13 under 510(k) number K022722. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PTA AND PTV?

PTA AND PTV is a medical device that received FDA 510(k) clearance on 2002-09-13. The listed applicant is NuMED, Inc.. The 510(k) number is K022722.

When did PTA AND PTV receive FDA 510(k) clearance?

PTA AND PTV received FDA 510(k) clearance on 2002-09-13, under 510(k) number K022722.

Who is the listed applicant for PTA AND PTV?

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

What is the FDA product code for PTA AND PTV?

The FDA product code for PTA AND PTV is DQY.

Other records listing NuMED, 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.

K213915BIB Stent Placement CatheterK211910Z-6 Atrioseptostomy CatheterK211134BIB Stent Placement CatheterK190974D'Vill IntroducerK171206D'Vill IntroducerK161451BIB Stent Placement Catheter

View all 48 devices →

Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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.

↑