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FDA 510(k)

INJECTION CAP

K-Number: K834480 · 1984-02-04

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1984-02-04
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INJECTION CAP 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 1984-02-04 under 510(k) number K834480. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INJECTION CAP?

INJECTION CAP is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K834480.

When did INJECTION CAP receive FDA 510(k) clearance?

INJECTION CAP received FDA 510(k) clearance on 1984-02-04, under 510(k) number K834480.

Who is the listed applicant for INJECTION CAP?

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 INJECTION CAP?

The FDA product code for INJECTION CAP is FOZ.

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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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