510(k) K831187
K831187 is an FDA 510(k) premarket notification submitted by Dms Laboratories for the device "TRP". The FDA issued a decision of Substantially Equivalent on May 9, 1983. The device falls under product code JTO (Discs, Strips And Reagents, Microorganism Differentiation), a Class I device regulated under 21 CFR 866.2660. Dms Laboratories has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 9, 1983
- Date Received
- April 12, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Discs, Strips And Reagents, Microorganism Differentiation
- Device Class
- Class I
- Regulation Number
- 866.2660
- Review Panel
- MI
- Submission Type