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FDA 510(k)

PERFUSION CATHETER

K-Number: K872790 · 1987-09-15

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1987-09-15
Product CodeDQT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

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 1987-09-15 under 510(k) number K872790. 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 PERFUSION CATHETER?

PERFUSION CATHETER is a medical device that received FDA 510(k) clearance on 1987-09-15. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K872790.

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

PERFUSION CATHETER received FDA 510(k) clearance on 1987-09-15, under 510(k) number K872790.

Who is the listed applicant for 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 PERFUSION CATHETER?

The FDA product code for PERFUSION CATHETER is DQT.

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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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