The following data is part of a premarket notification filed by Angiodynamics, Inc. with the FDA for Uniblate Electrosurgical Device.
| Device ID | K080451 |
| 510k Number | K080451 |
| Device Name: | UNIBLATE ELECTROSURGICAL DEVICE |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | ANGIODYNAMICS, INC. 603 QUEENSBURY AVE. Queensbury, NY 12804 |
| Contact | Brian Kunst |
| Correspondent | Brian Kunst ANGIODYNAMICS, INC. 603 QUEENSBURY AVE. Queensbury, NY 12804 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-02-19 |
| Decision Date | 2008-07-03 |
| Summary: | summary |