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FDA 510(k)

AUTOMATED PHYSIOLOGIC PROFILER

K-Number: K780530 · 1978-04-28

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1978-04-28
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AUTOMATED PHYSIOLOGIC PROFILER 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 1978-04-28 under 510(k) number K780530. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATED PHYSIOLOGIC PROFILER?

AUTOMATED PHYSIOLOGIC PROFILER is a medical device that received FDA 510(k) clearance on 1978-04-28. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K780530.

When did AUTOMATED PHYSIOLOGIC PROFILER receive FDA 510(k) clearance?

AUTOMATED PHYSIOLOGIC PROFILER received FDA 510(k) clearance on 1978-04-28, under 510(k) number K780530.

Who is the listed applicant for AUTOMATED PHYSIOLOGIC PROFILER?

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 AUTOMATED PHYSIOLOGIC PROFILER?

The FDA product code for AUTOMATED PHYSIOLOGIC PROFILER is DQK.

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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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