510(k) K112998
K112998 is an FDA 510(k) premarket notification submitted by Zoll Circulation for the device "AUTOPULSE RESUSCITATION SYSTEM MODEL 1000". The FDA issued a decision of Substantially Equivalent on March 15, 2012. The device falls under product code DRM (Compressor, Cardiac, External), a Class II device regulated under 21 CFR 870.5200. Zoll Circulation has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 15, 2012
- Date Received
- October 7, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Compressor, Cardiac, External
- Device Class
- Class II
- Regulation Number
- 870.5200
- Review Panel
- CV
- Submission Type