The following data is part of a premarket notification filed by Confluent Surgical,inc with the FDA for Confluent Surgical Dual Liquid Applicator, Model 70-2005-093.
| Device ID | K061183 |
| 510k Number | K061183 |
| Device Name: | CONFLUENT SURGICAL DUAL LIQUID APPLICATOR, MODEL 70-2005-093 |
| Classification | Syringe, Piston |
| Applicant | CONFLUENT SURGICAL,INC 101A FIRST AVE. Waltham, MA 02451 |
| Contact | Eric P Ankerud |
| Correspondent | Eric P Ankerud CONFLUENT SURGICAL,INC 101A FIRST AVE. Waltham, MA 02451 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-04-28 |
| Decision Date | 2006-06-01 |
| Summary: | summary |