510(k) K993200
K993200 is an FDA 510(k) premarket notification submitted by Isopure, Corp. for the device "MD 420/440/460/470/480/490". The FDA issued a decision of Substantially Equivalent on January 24, 2000. The device falls under product code FIP (Subsystem, Water Purification), a Class II device regulated under 21 CFR 876.5665. Isopure, Corp. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 24, 2000
- Date Received
- September 24, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Subsystem, Water Purification
- Device Class
- Class II
- Regulation Number
- 876.5665
- Review Panel
- GU
- Submission Type