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FDA 510(k)

VASCULAR CATHETER

K-Number: K831191 · 1983-05-09

ApplicantMedrad, Inc.
Decision Date1983-05-09
Product CodeDOY
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

VASCULAR CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 1983-05-09 under 510(k) number K831191. The device is classified under product code DOY. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCULAR CATHETER?

VASCULAR CATHETER is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Medrad, Inc.. The 510(k) number is K831191.

When did VASCULAR CATHETER receive FDA 510(k) clearance?

VASCULAR CATHETER received FDA 510(k) clearance on 1983-05-09, under 510(k) number K831191.

Who is the listed applicant for VASCULAR CATHETER?

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

What is the FDA product code for VASCULAR CATHETER?

The FDA product code for VASCULAR CATHETER is DOY.

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Other records listing Medrad, Inc. as applicant

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Related Devices (Code: DOY)

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.

K910154USCI ILLUMEN-8 8F PTCA GUIDING CATHETERC.R. Bard, Inc.K832396CENTRAL VENOUS ACCESS CATHETER CVACGish Biomedical, Inc.K831239WALRUS PERCUTANEOUS INTRODUCER SETMedical Parameters, Inc.K831188CONNECTOR TUBEMedrad, 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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