510(k) K860283
K860283 is an FDA 510(k) premarket notification submitted by Andover Medical, Inc. for the device "AMI CARDIO-PAD". The FDA issued a decision of Substantially Equivalent on March 31, 1986. The device falls under product code DRO (Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)), a Class II device regulated under 21 CFR 870.5550. Andover Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 31, 1986
- Date Received
- January 28, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
- Device Class
- Class II
- Regulation Number
- 870.5550
- Review Panel
- CV
- Submission Type