The following data is part of a premarket notification filed by Dms-service Llc with the FDA for My Patch Sl.
Device ID | K163535 |
510k Number | K163535 |
Device Name: | My Patch Sl |
Classification | Recorder, Magnetic Tape, Medical |
Applicant | DMS-SERVICE LLC 11845 W OLYMPIC BLVD STE 880W Los Angeles, CA 90064 |
Contact | Lynda Cole |
Correspondent | Lynda Cole DMS-SERVICE LLC 11845 W OLYMPIC BLVD STE 880W Los Angeles, CA 90064 |
Product Code | DSH |
CFR Regulation Number | 870.2800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-12-16 |
Decision Date | 2017-02-22 |
Summary: | summary |