The following data is part of a premarket notification filed by Computer Motion, Inc. with the FDA for Hermes Control Center, With Control Of The Aesop 3000hr (hermes Ready)..
| Device ID | K991444 |
| 510k Number | K991444 |
| Device Name: | HERMES CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERMES READY). |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | COMPUTER MOTION, INC. 130-B CREMONA DR. Goleta, CA 93117 |
| Contact | David Thomas |
| Correspondent | David Thomas COMPUTER MOTION, INC. 130-B CREMONA DR. Goleta, CA 93117 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-04-26 |
| Decision Date | 1999-06-25 |
| Summary: | summary |