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FDA 510(k)

VAC-RITE

K-Number: K885334 · 1989-03-08

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1989-03-08
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VAC-RITE 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 1989-03-08 under 510(k) number K885334. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAC-RITE?

VAC-RITE is a medical device that received FDA 510(k) clearance on 1989-03-08. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K885334.

When did VAC-RITE receive FDA 510(k) clearance?

VAC-RITE received FDA 510(k) clearance on 1989-03-08, under 510(k) number K885334.

Who is the listed applicant for VAC-RITE?

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 VAC-RITE?

The FDA product code for VAC-RITE is GCX.

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Related Devices (Code: GCX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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