The following data is part of a premarket notification filed by Schiff & Co. with the FDA for Kemble Liquid Handling System Dispenser.
| Device ID | K896684 |
| 510k Number | K896684 |
| Device Name: | KEMBLE LIQUID HANDLING SYSTEM DISPENSER |
| Classification | Station, Pipetting And Diluting, For Clinical Use |
| Applicant | SCHIFF & CO. 1129 BLOOMFIELD AVE. West Caldwell, NJ 07006 |
| Contact | Lauri A Kierstead |
| Correspondent | Lauri A Kierstead SCHIFF & CO. 1129 BLOOMFIELD AVE. West Caldwell, NJ 07006 |
| Product Code | JQW |
| CFR Regulation Number | 862.2750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-11-28 |
| Decision Date | 1990-04-16 |