BD BACTEC Standard/10 Aerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial

FDA 510(k) K161810 · Becton Dickinson

Substantially Equivalent

510(k) numberK161810

Submission

Device name
BD BACTEC Standard/10 Aerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial
Applicant
Becton Dickinson
Sparks, MD, US
Received
July 1, 2016
Decision date
February 9, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MDB – System, Blood Culturing
Device class
Class I (low risk)
Regulation
21 CFR 866.2560
Specialty
Microbiology

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Questions and answers

When was BD BACTEC Standard/10 Aerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial cleared by the FDA?

BD BACTEC Standard/10 Aerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial (K161810) received a 510(k) decision of Substantially Equivalent on February 9, 2017, 223 days after the submission was received.

What is the product code of K161810?

The FDA product code is MDB – System, Blood Culturing, a Class I (low risk) device regulated under 21 CFR 866.2560.