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FDA 510(k)

DIATROL BLOOD GLUCOSE TEST SYS

K-Number: K842684 · 1984-09-07

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1984-09-07
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIATROL BLOOD GLUCOSE TEST SYS 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 1984-09-07 under 510(k) number K842684. The device is classified under product code CGA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIATROL BLOOD GLUCOSE TEST SYS?

DIATROL BLOOD GLUCOSE TEST SYS is a medical device that received FDA 510(k) clearance on 1984-09-07. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K842684.

When did DIATROL BLOOD GLUCOSE TEST SYS receive FDA 510(k) clearance?

DIATROL BLOOD GLUCOSE TEST SYS received FDA 510(k) clearance on 1984-09-07, under 510(k) number K842684.

Who is the listed applicant for DIATROL BLOOD GLUCOSE TEST SYS?

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 DIATROL BLOOD GLUCOSE TEST SYS?

The FDA product code for DIATROL BLOOD GLUCOSE TEST SYS is CGA.

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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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