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FDA 510(k)

VAC-RITE SUNCTION COLLECTION

K-Number: K811192 · 1981-06-02

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1981-06-02
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VAC-RITE SUNCTION COLLECTION 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 1981-06-02 under 510(k) number K811192. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAC-RITE SUNCTION COLLECTION?

VAC-RITE SUNCTION COLLECTION is a medical device that received FDA 510(k) clearance on 1981-06-02. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K811192.

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

VAC-RITE SUNCTION COLLECTION received FDA 510(k) clearance on 1981-06-02, under 510(k) number K811192.

Who is the listed applicant for VAC-RITE SUNCTION COLLECTION?

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 SUNCTION COLLECTION?

The FDA product code for VAC-RITE SUNCTION COLLECTION is KDQ.

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Related Devices (Code: KDQ)

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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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