The following data is part of a premarket notification filed by Dentsleeve Pty., Ltd. with the FDA for Manometric Assemblies.
| Device ID | K983665 |
| 510k Number | K983665 |
| Device Name: | MANOMETRIC ASSEMBLIES |
| Classification | Monitor, Esophageal Motility, And Tube |
| Applicant | DENTSLEEVE PTY., LTD. 56 A/B GLEN OSMOND RD. Parkside South Australia, AU 5063 |
| Contact | Marcus Tippett |
| Correspondent | Marcus Tippett DENTSLEEVE PTY., LTD. 56 A/B GLEN OSMOND RD. Parkside South Australia, AU 5063 |
| Product Code | KLA |
| CFR Regulation Number | 876.1725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-10-19 |
| Decision Date | 1999-05-17 |
| Summary: | summary |