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BD BACTEC PLUS ANAEROBIC/F (PLASTIC)

K141810 Class I Traditional
Decision Date
2014-12-10
Sponsor / Applicant
Becton, Dickinson and Company

Technical Specification

510(k) Submission ID K141810
Product Code MDB
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.2560
Decision Date 2014-12-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BD BACTEC PLUS ANAEROBIC/F (PLASTIC) received FDA 510(k) clearance under submission number K141810, sponsored by Becton, Dickinson and Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2014-12-10.

Classification & Regulation

This clearance is catalogued under FDA product code MDB and 21 CFR 866.2560, within the Microbiology review panel as a Class I device.