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 |