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FDA 510(k)

BARD PARKER PERFUSION CATHETER

K-Number: K855201 · 1986-04-29

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1986-04-29
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BARD PARKER PERFUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1986-04-29 under 510(k) number K855201. 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 BARD PARKER PERFUSION CATHETER?

BARD PARKER PERFUSION CATHETER is a medical device that received FDA 510(k) clearance on 1986-04-29. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K855201.

When did BARD PARKER PERFUSION CATHETER receive FDA 510(k) clearance?

BARD PARKER PERFUSION CATHETER received FDA 510(k) clearance on 1986-04-29, under 510(k) number K855201.

Who is the listed applicant for BARD PARKER PERFUSION CATHETER?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARD PARKER PERFUSION CATHETER?

The FDA product code for BARD PARKER PERFUSION CATHETER is DQY.

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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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