510(k) K923497
K923497 is an FDA 510(k) premarket notification submitted by Orion Life Systems, Inc. for the device "FLUSHING IRRIGATION SET". The FDA issued a decision of Substantially Equivalent (kit) on March 21, 1994. The device falls under product code KDH (Catheter (Gastric, Colonic, Etc.), Irrigation And Aspiration), a Class II device regulated under 21 CFR 876.5980. Orion Life Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESK (Substantially Equivalent (kit))
- Decision Date
- March 21, 1994
- Date Received
- July 15, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter (Gastric, Colonic, Etc.), Irrigation And Aspiration
- Device Class
- Class II
- Regulation Number
- 876.5980
- Review Panel
- GU
- Submission Type