FDA 510(k)

ACRIDINE ORANGE STAIN

K-Number: K810040 · 1981-02-12

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1981-02-12

Product CodeIDC

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

ACRIDINE ORANGE STAIN 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 1981-02-12 under 510(k) number K810040. The device is classified under product code IDC. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACRIDINE ORANGE STAIN?

ACRIDINE ORANGE STAIN is a medical device that received FDA 510(k) clearance on 1981-02-12. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K810040.

When did ACRIDINE ORANGE STAIN receive FDA 510(k) clearance?

ACRIDINE ORANGE STAIN received FDA 510(k) clearance on 1981-02-12, under 510(k) number K810040.

Who is the listed applicant for ACRIDINE ORANGE STAIN?

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 ACRIDINE ORANGE STAIN?

The FDA product code for ACRIDINE ORANGE STAIN is IDC.

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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.