510(k) K893612
K893612 is an FDA 510(k) premarket notification submitted by National Medical Care, Medical Products Div., Inc. for the device "TWO TANK DISSOLUTION MODULE". The FDA issued a decision of Substantially Equivalent on July 24, 1989. The device falls under product code FKQ (System, Dialysate Delivery, Central Multiple Patient), a Class II device regulated under 21 CFR 876.5820. National Medical Care, Medical Products Div., Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 24, 1989
- Date Received
- May 10, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Dialysate Delivery, Central Multiple Patient
- Device Class
- Class II
- Regulation Number
- 876.5820
- Review Panel
- GU
- Submission Type