510(k) K811217
K811217 is an FDA 510(k) premarket notification submitted by Cardiac Pacemakers, Inc. for the device "PACEMAKER PROGRAMMER #2010". The FDA issued a decision of Substantially Equivalent on July 20, 1981. The device falls under product code KRG (Programmer, Pacemaker), a Class III device regulated under 21 CFR 870.3700. Cardiac Pacemakers, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 20, 1981
- Date Received
- May 4, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Programmer, Pacemaker
- Device Class
- Class III
- Regulation Number
- 870.3700
- Review Panel
- CV
- Submission Type