Channel Medsystems

FDA Filings

This page includes the latest FDA filings for Channel Medsystems. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3012018285
• FEI Number: 3012018285
• Name: CHANNEL MEDSYSTEMS
• Owner & Operator: Channel Medsystems
• Contact Address: Channel Medsystems 5858 Horton Street, Suite 200; Emeryville CA 94608 US
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 5858 Horton Street Suite 200; Emeryville, CA 94608 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN P180032 | MNB CHANNEL MEDSYSTEMS	Exhaust Collection Bag	2019-04-03
PMN P180032 | MNB CHANNEL MEDSYSTEMS	Cerene Cryotherapy Device	2019-04-03

Similar & Related FDA Registered Companies

• Channel Medsystems, Inc.5858 Horton Street, Suite 200emeryville, CA 94608 PMA NumberP180032 Supplement NumberS011 Date Received12/21/2022 Decision Date01/17/2023 Product Code MNB  Advisory Committee Obstetrics/Gynecology Supplement Typespecial (immediate Track) Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• Channel Medsystems, Inc.5858 Horton Street, Suite 200emeryville, CA 94608 PMA NumberP180032 Supplement NumberS010 Date Received05/02/2022 Decision Date05/31/2022 Product Code MNB  Advisory Committee Obstetrics/Gynecology Supplement Typespecial (immediate Track) Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• Channel Medsystems, Inc.