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FDA 510(k)

MEDX 1000 SERIES

K-Number: K020017 · 2002-07-12

ApplicantMedx Electronics, Inc.
Decision Date2002-07-12
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDX 1000 SERIES 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 2002-07-12 under 510(k) number K020017. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDX 1000 SERIES?

MEDX 1000 SERIES is a medical device that received FDA 510(k) clearance on 2002-07-12. The listed applicant is Medx Electronics, Inc.. The 510(k) number is K020017.

When did MEDX 1000 SERIES receive FDA 510(k) clearance?

MEDX 1000 SERIES received FDA 510(k) clearance on 2002-07-12, under 510(k) number K020017.

Who is the listed applicant for MEDX 1000 SERIES?

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 MEDX 1000 SERIES?

The FDA product code for MEDX 1000 SERIES is ILY.

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Other records listing Medx Electronics, Inc. as applicant

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.

K082707MEDX LPT 200 TETHERED LASER & MEDX LPS 200 (ORALASE) PORTABLE LASERK050022MEDX HOMEK032231MEDX1100 CONSOLE & MEDX 100T AND DUOLIGHT LASER ACCESSORIES, MEDX 100 PORTABLE LASERK024310NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORYK021985MEDX LCS LASER SERIES

Related Devices (Code: ILY)

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.

K253965CureLight Medical Diode Laser Systems (CureLight F2-A15; CureLight F2-B15; CureLight F2-A30; CureLight F2-B30; CureLight F3-AB30; CureLight F3-AB60.)Wuhan PHOMED Technology Company , Ltd.K242755Medical Diode Laser Systems (VELAS II-30B, VELAS II-30A, GBOX-15AB, GBOX-20B, CHEESE II-10B)Gigaalaser Company , Ltd.K231997SIRONA 100 Therapy Laser System (OEM's Model EVANLAS)Cure Point Therapeutics, Inc.K223642LED Lip Perfector, model: ZC-05Light Tree Ventures Europe B.V.K221189OLIZ LTB-1000ALtbio Co., Ltd.K213524CytonPro-5000Cytonsys, Inc.

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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