Becton Dickinson Safety-Lok Syringe

FDA 510(k) K920321 · Bd Becton Dickinson Vacutainer Systems Preanalytic

Substantially Equivalent

510(k) numberK920321

Submission

Device name
Becton Dickinson Safety-Lok Syringe
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Franklin Lakes, NJ, US
Received
January 24, 1992
Decision date
April 20, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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 Safety-Lok Syringe cleared by the FDA?

Becton Dickinson Safety-Lok Syringe (K920321) received a 510(k) decision of Substantially Equivalent on April 20, 1992, 87 days after the submission was received.

What is the product code of K920321?

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