The following data is part of a premarket notification filed by Aqueduct Critical Care, Inc. with the FDA for Smart External Drain (sed) System.
Device ID | K172759 |
510k Number | K172759 |
Device Name: | Smart External Drain (SED) System |
Classification | Shunt, Central Nervous System And Components |
Applicant | Aqueduct Critical Care, Inc. 11822 North Creek Parkway North Suite 110 Bothell, WA 98011 |
Contact | Thomas Clement |
Correspondent | Thomas Clement Aqueduct Critical Care, Inc. 11822 North Creek Parkway North Suite 110 Bothell, WA 98011 |
Product Code | JXG |
CFR Regulation Number | 882.5550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-09-13 |
Decision Date | 2017-11-14 |
Summary: | summary |