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 |