The following data is part of a premarket notification filed by Liger Medical, Llc with the FDA for Liger Medical Esu-110.
| Device ID | K133273 |
| 510k Number | K133273 |
| Device Name: | LIGER MEDICAL ESU-110 |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | LIGER MEDICAL, LLC 825 N 300 WEST #NE127 Salt Lake City, UT 84103 |
| Contact | Steve Smith |
| Correspondent | Steve Smith LIGER MEDICAL, LLC 825 N 300 WEST #NE127 Salt Lake City, UT 84103 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-10-24 |
| Decision Date | 2014-02-12 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00861592000300 | K133273 | 000 |