The following data is part of a premarket notification filed by Arbor Technologies, Inc. with the FDA for Syringefilter.
| Device ID | K960928 |
| 510k Number | K960928 |
| Device Name: | SYRINGEFILTER |
| Classification | Filter, Conduction, Anesthetic |
| Applicant | ARBOR TECHNOLOGIES, INC. 401 W. MORGAN RD. Ann Arbor, MI 48108 |
| Contact | Dawn I Moore |
| Correspondent | Dawn I Moore ARBOR TECHNOLOGIES, INC. 401 W. MORGAN RD. 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 | 1996-03-07 |
| Decision Date | 1997-04-04 |
| Summary: | summary |