The following data is part of a premarket notification filed by Arbor Technologies, Inc. with the FDA for Anesthesia Conduction Filter.
| Device ID | K902666 |
| 510k Number | K902666 |
| Device Name: | ANESTHESIA CONDUCTION FILTER |
| Classification | Filter, Conduction, Anesthetic |
| Applicant | ARBOR TECHNOLOGIES, INC. 3728 PLAZA DR. Ann Arbor, MI 48108 |
| Contact | Dawn I Moore |
| Correspondent | Dawn I Moore ARBOR TECHNOLOGIES, INC. 3728 PLAZA DR. Ann Arbor, MI 48108 |
| Product Code | BSN |
| CFR Regulation Number | 868.5130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-06-18 |
| Decision Date | 1991-04-23 |