510(k) K873725
K873725 is an FDA 510(k) premarket notification submitted by Simmler, Inc. for the device "MULTICHEM CREATININE REAGENT S0917". The FDA issued a decision of Substantially Equivalent on Oct 20, 1987. The device falls under product code CGX (Alkaline Picrate, Colorimetry, Creatinine), a Class II device regulated under 21 CFR 862.1225. Simmler, Inc. has 22 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 20, 1987
- Date Received
- Sep 15, 1987
- 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
- 510(k)