510(k) K890783
K890783 is an FDA 510(k) premarket notification submitted by Grieshaber & Co. for the device "GRIESHABER VISCOELASTIC INJECTION SYSTEM". The FDA issued a decision of Substantially Equivalent on May 16, 1989. The device falls under product code FRN (Pump, Infusion), a Class II device regulated under 21 CFR 880.5725. Grieshaber & Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 16, 1989
- Date Received
- February 15, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pump, Infusion
- Device Class
- Class II
- Regulation Number
- 880.5725
- Review Panel
- HO
- Submission Type