Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ETEST Piperacillin/Tazobactam (P/T) (0.016/4-256/4 ug/mL)

K-Number: K190154 · 2019-05-01

Decision Date2019-05-01
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ETEST Piperacillin/Tazobactam (P/T) (0.016/4-256/4 ug/mL) is a medical device manufactured by Biomerieux S.A.. It received FDA 510(k) clearance on 2019-05-01 under approval number K190154. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ETEST Piperacillin/Tazobactam (P/T) (0.016/4-256/4 ug/mL)?

ETEST Piperacillin/Tazobactam (P/T) (0.016/4-256/4 ug/mL) is a medical device that received FDA 510(k) clearance on 2019-05-01. It is manufactured by Biomerieux S.A.. The 510(k) number is K190154.

When was ETEST Piperacillin/Tazobactam (P/T) (0.016/4-256/4 ug/mL) approved by the FDA?

ETEST Piperacillin/Tazobactam (P/T) (0.016/4-256/4 ug/mL) received FDA 510(k) clearance on 2019-05-01, under approval number K190154.

What company makes ETEST Piperacillin/Tazobactam (P/T) (0.016/4-256/4 ug/mL)?

ETEST Piperacillin/Tazobactam (P/T) (0.016/4-256/4 ug/mL) is manufactured by Biomerieux S.A..

What is the FDA product code for ETEST Piperacillin/Tazobactam (P/T) (0.016/4-256/4 ug/mL)?

The FDA product code for ETEST Piperacillin/Tazobactam (P/T) (0.016/4-256/4 ug/mL) is JWY.

Other Devices by Biomerieux S.A.

View all 10 devices →

Related Devices (Code: JWY)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.