510(k) K171942
K171942 is an FDA 510(k) premarket notification submitted by Edan Instruments, Inc. for the device "Electrocardiograph". The FDA issued a decision of Substantially Equivalent on Jan 24, 2018. The device falls under product code DPS (Electrocardiograph), a Class II device regulated under 21 CFR 870.2340. Edan Instruments, Inc. has 93 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 24, 2018
- Date Received
- Jun 28, 2017
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrocardiograph
- Device Class
- Class II
- Regulation Number
- 870.2340
- Review Panel
- CV
- Submission Type
- 510(k)