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FDA 510(k)

Single Use Arthroscopic Electrode (with Pencil)

K-Number: K170703 · 2018-05-31

ApplicantModern Medical Equipment Manufacturing Limited
Decision Date2018-05-31
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Single Use Arthroscopic Electrode (with Pencil) is the device name listed in this FDA 510(k) record. The listed applicant is Modern Medical Equipment Manufacturing Limited. It received FDA 510(k) clearance on 2018-05-31 under 510(k) 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. The listed applicant is Modern Medical Equipment Manufacturing Limited. The 510(k) number is K170703.

When did Single Use Arthroscopic Electrode (with Pencil) receive FDA 510(k) clearance?

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

Who is the listed applicant for Single Use Arthroscopic Electrode (with Pencil)?

The FDA 510(k) record lists Modern Medical Equipment Manufacturing Limited as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Modern Medical Equipment Manufacturing Limited as applicant

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Related Devices (Code: HRX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252790Digital ClarusScope System and Digital NeuroPEN SystemClarus Medical, LLCK253523Freedom DS™ Decompression SystemSpinal SimplicityK252546VantageTM Lumbar Decompression KitAllevion Medical, LLCK253217MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)Medimaging Integrated Solution, Inc (Miis)K250795PUREVUE™ FMSW.O.M. World of Medicine GmbHK252666Articulator Arthroscopic BurJoint Preservation Innovations, LLC

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.

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