510(k) K932619
K932619 is an FDA 510(k) premarket notification submitted by Thomas Medical Products, Inc. for the device "TRANSSEPTAL INTRODUCER SET". The FDA issued a decision of Substantially Equivalent on August 24, 1993. The device falls under product code DQY (Catheter, Percutaneous), a Class II device regulated under 21 CFR 870.1250. Thomas Medical Products, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 24, 1993
- Date Received
- June 1, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Percutaneous
- Device Class
- Class II
- Regulation Number
- 870.1250
- Review Panel
- CV
- Submission Type