The following data is part of a premarket notification filed by Arbor Technologies, Inc. with the FDA for Contain(tm).
| Device ID | K895859 |
| 510k Number | K895859 |
| Device Name: | CONTAIN(TM) |
| Classification | Apparatus, Suction, Operating-room, Wall Vacuum Powered |
| 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 | GCX |
| CFR Regulation Number | 880.6740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-10-03 |
| Decision Date | 1991-02-07 |