510(k) K935179
K935179 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "EMDS ALBUMIN (ALB) TEST". The FDA issued a decision of Substantially Equivalent on December 17, 1993. The device falls under product code CIX (Bromcresol Green Dye-Binding, Albumin), a Class II device regulated under 21 CFR 862.1035. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 17, 1993
- Date Received
- October 26, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Bromcresol Green Dye-Binding, Albumin
- Device Class
- Class II
- Regulation Number
- 862.1035
- Review Panel
- CH
- Submission Type