510(k) K871208
K871208 is an FDA 510(k) premarket notification submitted by Pacesetter Systems for the device "UNIPOLAR ENDOCARDIAL SCREW-IN LEAD, MODEL 1007M". The FDA issued a decision of Substantially Equivalent on June 5, 1987. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. Pacesetter Systems has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 5, 1987
- Date Received
- March 25, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Introducer, Catheter
- Device Class
- Class II
- Regulation Number
- 870.1340
- Review Panel
- CV
- Submission Type