510(k) K851611
K851611 is an FDA 510(k) premarket notification submitted by Impact Instrumentation, Inc. for the device "IMPACT TURBO CATH". The FDA issued a decision of Substantially Equivalent on June 5, 1985. The device falls under product code JOL (Catheter And Tip, Suction), a Class II device regulated under 21 CFR 880.6740. Impact Instrumentation, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 5, 1985
- Date Received
- April 9, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter And Tip, Suction
- Device Class
- Class II
- Regulation Number
- 880.6740
- Review Panel
- HO
- Submission Type