PATIENT MONITOR

Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms)

EDAN INSTRUMENTS INC

The following data is part of a premarket notification filed by Edan Instruments Inc with the FDA for Patient Monitor.

Pre-market Notification Details

• Device ID: K120173
• 510k Number: K120173
• Device Name: PATIENT MONITOR
• Classification: Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms)
• Applicant: EDAN INSTRUMENTS INC 3/F-B, NANSHAN MEDICAL EQUIPMENTS PARK Shenzhen, CN 518067
• Contact: Randy Jiang
• Correspondent: Randy Jiang; EDAN INSTRUMENTS INC 3/F-B, NANSHAN MEDICAL EQUIPMENTS PARK Shenzhen, CN 518067
• Product Code: MHX
• Subsequent Product Code: CBQ
• Subsequent Product Code: CBR
• Subsequent Product Code: CBS
• Subsequent Product Code: CCK
• Subsequent Product Code: CCL
• Subsequent Product Code: DQA
• Subsequent Product Code: DRT
• Subsequent Product Code: DSA
• Subsequent Product Code: DSI
• Subsequent Product Code: DSK
• Subsequent Product Code: DXN
• Subsequent Product Code: FLL
• Subsequent Product Code: MLD
• CFR Regulation Number: 870.1025 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2012-01-20
• Decision Date: 2012-05-16
• Summary: summary