510(k) K894131
K894131 is an FDA 510(k) premarket notification submitted by Thermedics, Inc. for the device "DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000". The FDA issued a decision of Substantially Equivalent on September 26, 1989. The device falls under product code DQY (Catheter, Percutaneous), a Class II device regulated under 21 CFR 870.1250. Thermedics, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 26, 1989
- Date Received
- June 13, 1989
- 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