The following data is part of a premarket notification filed by Hoggan Scientific, Llc with the FDA for Hoggan Scientific® Microfet2™.
| Device ID | K162412 |
| 510k Number | K162412 |
| Device Name: | Hoggan Scientific® MicroFET2™ |
| Classification | Dynamometer, Ac-powered |
| Applicant | Hoggan Scientific, LLC 3653 West 1987 South Bld. # 7 Salt Lake City, UT 84104 |
| Contact | Spencer Walker |
| Correspondent | Spencer Walker Hoggan Scientific, LLC 3653 West 1987 South Bld. # 7 Salt Lake City, UT 84104 |
| Product Code | LBB |
| CFR Regulation Number | 888.1240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-08-29 |
| Decision Date | 2017-03-09 |
| Summary: | summary |