The following data is part of a premarket notification filed by Aspen Labs with the FDA for Electrosurgical Unit With Accessories.
Device ID | K905654 |
510k Number | K905654 |
Device Name: | ELECTROSURGICAL UNIT WITH ACCESSORIES |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | ASPEN LABS P.O. BOX 3936 Englewood, CO 80155 |
Contact | Jane Johnson |
Correspondent | Jane Johnson ASPEN LABS P.O. BOX 3936 Englewood, CO 80155 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-12-18 |
Decision Date | 1991-03-18 |