510(k) K070504
K070504 is an FDA 510(k) premarket notification submitted by Pointe Scientific, Inc., for the device "AMMONIA/ALCOHOL CONTROL SET". The FDA issued a decision of Substantially Equivalent on April 11, 2007. The device falls under product code JJY (Multi-Analyte Controls, All Kinds (Assayed)), a Class I device regulated under 21 CFR 862.1660. Pointe Scientific, Inc., has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 11, 2007
- Date Received
- February 21, 2007
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Multi-Analyte Controls, All Kinds (Assayed)
- Device Class
- Class I
- Regulation Number
- 862.1660
- Review Panel
- CH
- Submission Type