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FDA 510(k)

UPSTREAM GR CATHETER

K-Number: K120964 · 2012-05-25

ApplicantUpstream Peripheral Technologies
Decision Date2012-05-25
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

UPSTREAM GR CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Upstream Peripheral Technologies. It received FDA 510(k) clearance on 2012-05-25 under 510(k) number K120964. 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 UPSTREAM GR CATHETER?

UPSTREAM GR CATHETER is a medical device that received FDA 510(k) clearance on 2012-05-25. The listed applicant is Upstream Peripheral Technologies. The 510(k) number is K120964.

When did UPSTREAM GR CATHETER receive FDA 510(k) clearance?

UPSTREAM GR CATHETER received FDA 510(k) clearance on 2012-05-25, under 510(k) number K120964.

Who is the listed applicant for UPSTREAM GR CATHETER?

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

What is the FDA product code for UPSTREAM GR CATHETER?

The FDA product code for UPSTREAM GR CATHETER is DQY.

Related Clinical Trials

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.

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Other records listing Upstream Peripheral Technologies 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.

K112887UPSTREAM NEEDLE HOLDER, UPSTREAM NEEDLE HOLDER WITH SHUT-OFF CONNECTORK112886UPSTREAM SUPPORT CATHETER

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.

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