510(k) K130785
K130785 is an FDA 510(k) premarket notification submitted by Getemed Medizin- Und Informationstechnik AG for the device "SEER 1000". The FDA issued a decision of Substantially Equivalent on July 26, 2013. The device falls under product code MWJ (Electrocardiograph, Ambulatory (Without Analysis)), a Class II device regulated under 21 CFR 870.2800. Getemed Medizin- Und Informationstechnik AG has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 26, 2013
- Date Received
- March 21, 2013
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrocardiograph, Ambulatory (Without Analysis)
- Device Class
- Class II
- Regulation Number
- 870.2800
- Review Panel
- CV
- Submission Type