510(k) K925038
K925038 is an FDA 510(k) premarket notification submitted by Siemens-Pacesetter, Inc. for the device "PACING LEAD MODEL 1188T". The FDA issued a decision of ST on July 15, 1994. The device falls under product code DTB (Permanent Pacemaker Electrode), a Class III device regulated under 21 CFR 870.3680. Siemens-Pacesetter, Inc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- ST ()
- Decision Date
- July 15, 1994
- Date Received
- October 5, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Permanent Pacemaker Electrode
- Device Class
- Class III
- Regulation Number
- 870.3680
- Review Panel
- CV
- Submission Type