FDA 510(k)

I.V. STARTPAK VASCULAR ACCESS START KIT

K-Number: K942238 · 1994-06-03

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1994-06-03

Product CodeLRS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

I.V. STARTPAK VASCULAR ACCESS START KIT 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 1994-06-03 under 510(k) number K942238. The device is classified under product code LRS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.V. STARTPAK VASCULAR ACCESS START KIT?

I.V. STARTPAK VASCULAR ACCESS START KIT is a medical device that received FDA 510(k) clearance on 1994-06-03. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K942238.

When did I.V. STARTPAK VASCULAR ACCESS START KIT receive FDA 510(k) clearance?

I.V. STARTPAK VASCULAR ACCESS START KIT received FDA 510(k) clearance on 1994-06-03, under 510(k) number K942238.

Who is the listed applicant for I.V. STARTPAK VASCULAR ACCESS START KIT?

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 I.V. STARTPAK VASCULAR ACCESS START KIT?

The FDA product code for I.V. STARTPAK VASCULAR ACCESS START KIT is LRS.

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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.