BD Preset Blood Collection Syringe, BD A-Line Blood Collection Syringe, Models 365313, 365323,365316,365356,365373,36538

FDA 510(k) K022426 · Becton, Dickinson & CO

Substantially Equivalent

510(k) numberK022426

Submission

Device name
BD Preset Blood Collection Syringe, BD A-Line Blood Collection Syringe, Models 365313, 365323,365316,365356,365373,36538
Applicant
Becton, Dickinson & CO
Franklin Lakes, NJ, US
Received
July 25, 2002
Decision date
August 8, 2002
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JKA – Tubes, Vials, Systems, Serum Separators, Blood Collection
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1675
Specialty
Clinical Chemistry

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Questions and answers

When was BD Preset Blood Collection Syringe, BD A-Line Blood Collection Syringe, Models 365313, 365323,365316,365356,365373,36538 cleared by the FDA?

BD Preset Blood Collection Syringe, BD A-Line Blood Collection Syringe, Models 365313, 365323,365316,365356,365373,36538 (K022426) received a 510(k) decision of Substantially Equivalent on August 8, 2002, 14 days after the submission was received.

What is the product code of K022426?

The FDA product code is JKA – Tubes, Vials, Systems, Serum Separators, Blood Collection, a Class II (moderate risk) device regulated under 21 CFR 862.1675.