Becton Dickinson Dispos. Syringes Plunger Tip Mod.

FDA 510(k) K930321 · Bd Becton Dickinson Vacutainer Systems Preanalytic

Substantially Equivalent

510(k) numberK930321

Submission

Device name
Becton Dickinson Dispos. Syringes Plunger Tip Mod.
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Franklin Lakes, NJ, US
Received
January 22, 1993
Decision date
May 17, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMF – Syringe, Piston
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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Questions and answers

When was Becton Dickinson Dispos. Syringes Plunger Tip Mod. cleared by the FDA?

Becton Dickinson Dispos. Syringes Plunger Tip Mod. (K930321) received a 510(k) decision of Substantially Equivalent on May 17, 1993, 115 days after the submission was received.

What is the product code of K930321?

The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.