FDA 510(k)

BD MICROFINE IV PEN INJECTOR

K-Number: K881775 · 1988-08-23

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1988-08-23

Product CodeFMF

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BD MICROFINE IV PEN INJECTOR 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 1988-08-23 under 510(k) number K881775. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD MICROFINE IV PEN INJECTOR?

BD MICROFINE IV PEN INJECTOR is a medical device that received FDA 510(k) clearance on 1988-08-23. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K881775.

When did BD MICROFINE IV PEN INJECTOR receive FDA 510(k) clearance?

BD MICROFINE IV PEN INJECTOR received FDA 510(k) clearance on 1988-08-23, under 510(k) number K881775.

Who is the listed applicant for BD MICROFINE IV PEN INJECTOR?

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 BD MICROFINE IV PEN INJECTOR?

The FDA product code for BD MICROFINE IV PEN INJECTOR is FMF.

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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.