510(k) K983937
K983937 is an FDA 510(k) premarket notification submitted by Intersect Systems, Inc. for the device "DUAL VIAL CREATININE REAGENT". The FDA issued a decision of Substantially Equivalent on January 6, 1999. The device falls under product code CGX (Alkaline Picrate, Colorimetry, Creatinine), a Class II device regulated under 21 CFR 862.1225. Intersect Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 6, 1999
- Date Received
- November 5, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Alkaline Picrate, Colorimetry, Creatinine
- Device Class
- Class II
- Regulation Number
- 862.1225
- Review Panel
- CH
- Submission Type