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)

Single Use Arthroscopic Electrode (with Pencil)

K-Number: K170703 · 2018-05-31

Decision Date2018-05-31
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Single Use Arthroscopic Electrode (with Pencil) is a medical device manufactured by Modern Medical Equipment Manufacturing Limited. It received FDA 510(k) clearance on 2018-05-31 under approval number K170703. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Single Use Arthroscopic Electrode (with Pencil)?

Single Use Arthroscopic Electrode (with Pencil) is a medical device that received FDA 510(k) clearance on 2018-05-31. It is manufactured by Modern Medical Equipment Manufacturing Limited. The 510(k) number is K170703.

When was Single Use Arthroscopic Electrode (with Pencil) approved by the FDA?

Single Use Arthroscopic Electrode (with Pencil) received FDA 510(k) clearance on 2018-05-31, under approval number K170703.

What company makes Single Use Arthroscopic Electrode (with Pencil)?

Single Use Arthroscopic Electrode (with Pencil) is manufactured by Modern Medical Equipment Manufacturing Limited.

What is the FDA product code for Single Use Arthroscopic Electrode (with Pencil)?

The FDA product code for Single Use Arthroscopic Electrode (with Pencil) is HRX.

Related Clinical Trials

Other Devices by Modern Medical Equipment Manufacturing Limited

Related Devices (Code: HRX)

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.