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)

BOWA Neutral Electrodes

K-Number: K173877 · 2018-02-15

ApplicantBowa-Electronics GmbH & Co. KG
Decision Date2018-02-15
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BOWA Neutral Electrodes is a medical device manufactured by Bowa-Electronics GmbH & Co. KG. It received FDA 510(k) clearance on 2018-02-15 under approval number K173877. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOWA Neutral Electrodes?

BOWA Neutral Electrodes is a medical device that received FDA 510(k) clearance on 2018-02-15. It is manufactured by Bowa-Electronics GmbH & Co. KG. The 510(k) number is K173877.

When was BOWA Neutral Electrodes approved by the FDA?

BOWA Neutral Electrodes received FDA 510(k) clearance on 2018-02-15, under approval number K173877.

What company makes BOWA Neutral Electrodes?

BOWA Neutral Electrodes is manufactured by Bowa-Electronics GmbH & Co. KG.

What is the FDA product code for BOWA Neutral Electrodes?

The FDA product code for BOWA Neutral Electrodes is GEI.

Other Devices by Bowa-Electronics GmbH & Co. KG

K193591ARC 400

Related Devices (Code: GEI)

K161307NICO MyriadNico Corporation K163190InMode RF SystemInmode MD , Ltd. K163373PK AIMGyrus Acmi, Inc. K163106CODMAN Integrated Bipolar Cord and Tubing SetMedos International SARL K162676Voyant Open Fusion DeviceApplied Medical Resources K162941Ligasure Blunt Tip, Sealer/Divider, Nano-coatedCovidien

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.

↑