FDA 510(k)

BLOOD TUBING SETS

K-Number: K760042 · 1976-08-30

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1976-08-30

Product CodeKOC

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BLOOD TUBING SETS 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 1976-08-30 under 510(k) number K760042. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD TUBING SETS?

BLOOD TUBING SETS is a medical device that received FDA 510(k) clearance on 1976-08-30. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K760042.

When did BLOOD TUBING SETS receive FDA 510(k) clearance?

BLOOD TUBING SETS received FDA 510(k) clearance on 1976-08-30, under 510(k) number K760042.

Who is the listed applicant for BLOOD TUBING SETS?

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 BLOOD TUBING SETS?

The FDA product code for BLOOD TUBING SETS is KOC.

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Related Devices (Code: KOC)

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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.