510(k) K870704
K870704 is an FDA 510(k) premarket notification submitted by American Pharmaseal Div. Ahsc for the device "CLOSED PARACENTESIS SYSTEM W/BOASBERG CATHETER SET". The FDA issued a decision of Substantially Equivalent (with conditions) on March 27, 1987. The device falls under product code GBX (Catheter, Irrigation), a Class I device regulated under 21 CFR 878.4200. American Pharmaseal Div. Ahsc has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESD (Substantially Equivalent (with conditions))
- Decision Date
- March 27, 1987
- Date Received
- February 20, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Irrigation
- Device Class
- Class I
- Regulation Number
- 878.4200
- Review Panel
- SU
- Submission Type