510(k) K963073
K963073 is an FDA 510(k) premarket notification submitted by Harmac Medical Products, Inc. for the device "HARMAC BIPOLAR TEMPORARY PACING CATHETER WITH STYLET". The FDA issued a decision of Substantially Equivalent on August 14, 1997. The device falls under product code LDF (Electrode, Pacemaker, Temporary), a Class II device regulated under 21 CFR 870.3680. Harmac Medical Products, Inc. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 14, 1997
- Date Received
- June 28, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrode, Pacemaker, Temporary
- Device Class
- Class II
- Regulation Number
- 870.3680
- Review Panel
- CV
- Submission Type