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FDA 510(k)

NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORY

K-Number: K024310 · 2003-03-24

ApplicantMedx Electronics, Inc.
Decision Date2003-03-24
Product CodeNHN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Medx Electronics, Inc.. It received FDA 510(k) clearance on 2003-03-24 under 510(k) number K024310. The device is classified under product code NHN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORY?

NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORY is a medical device that received FDA 510(k) clearance on 2003-03-24. The listed applicant is Medx Electronics, Inc.. The 510(k) number is K024310.

When did NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORY receive FDA 510(k) clearance?

NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORY received FDA 510(k) clearance on 2003-03-24, under 510(k) number K024310.

Who is the listed applicant for NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORY?

The FDA 510(k) record lists Medx Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORY?

The FDA product code for NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORY is NHN.

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Other records listing Medx Electronics, Inc. as applicant

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K082707MEDX LPT 200 TETHERED LASER & MEDX LPS 200 (ORALASE) PORTABLE LASERK050022MEDX HOMEK032231MEDX1100 CONSOLE & MEDX 100T AND DUOLIGHT LASER ACCESSORIES, MEDX 100 PORTABLE LASERK021985MEDX LCS LASER SERIESK020017MEDX 1000 SERIES

Related Devices (Code: NHN)

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.

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Official Source

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

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