The following data is part of a premarket notification filed by Eclipse Medcorp Llc with the FDA for Micropen Evo.
Device ID | K212558 |
510k Number | K212558 |
Device Name: | MicroPen EVO |
Classification | Powered Microneedle Device |
Applicant | Eclipse Medcorp LLC 5916 Stone Creek Drive The Colony, TX 75056 |
Contact | Julie Summerville |
Correspondent | Julie Summerville Eclipse Medcorp LLC 5916 Stone Creek Drive The Colony, TX 75056 |
Product Code | QAI |
CFR Regulation Number | 878.4430 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-08-13 |
Decision Date | 2021-11-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MICROPEN EVO 90465541 not registered Live/Pending |
Eclipse MedCorp, LLC 2021-01-14 |
MICROPEN EVO 90465512 not registered Live/Pending |
Eclipse MedCorp, LLC 2021-01-14 |
MICROPEN EVO 88731960 not registered Live/Pending |
Eclipse MedCorp, LLC 2019-12-18 |