510(k) K031367
K031367 is an FDA 510(k) premarket notification submitted by Emd Chemicals, Inc. for the device "DUOPATH VEROTOXINS GLISA TEST". The FDA issued a decision of Substantially Equivalent on January 23, 2004. The device falls under product code GNA (Antisera, All Types, Escherichia Coli), a Class I device regulated under 21 CFR 866.3255. Emd Chemicals, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 23, 2004
- Date Received
- April 30, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antisera, All Types, Escherichia Coli
- Device Class
- Class I
- Regulation Number
- 866.3255
- Review Panel
- MI
- Submission Type