Data / Medical devices / Russia / Milta Pkp-Git
Milta Pkp-Git: FDA-registered device maker in Moscow Moskva, Russia, 3 510(k) clearances
Milta Pkp-Git is registered with the FDA (registration 3005739661) in Moscow Moskva, Russia. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 20, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005739661
- Address
- Borovaya str.,7 building 7 office 29, Moscow Moskva, Russia, 11102
- Owner or operator
- Multi Radiance Medical (9087202)
- Roles
- Manufacturer
- First device listed
- June 1, 2012
- Registered through
- 2026
- Brand names listed
- Contoura Laser Stim, LS50 Emitter, Laser STIM Target Emitter, Laser Shower LS50, Laser Stim, MR4 Activ, MR4 Laser, MR4 LaserShower 50 4-D Emitter and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 20, 2008 | K080102 | TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM | ILY | Substantially Equivalent | Escada International, Inc. | accessdata.fda.gov |
| October 29, 2007 | K071445 | TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS | ILY | Substantially Equivalent | Escada International, Inc. | accessdata.fda.gov |
| October 6, 2006 | K061614 | TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS | ILY | Substantially Equivalent | Escada International, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Powered Laser Surgical Instrument
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
Updated August 20, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.