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 |