510(k) K132091
K132091 is an FDA 510(k) premarket notification submitted by Techno-Path Manufacturing , Ltd. for the device "MULTICHEM IA AND IA PLUS". The FDA issued a decision of Substantially Equivalent on September 20, 2013. The device falls under product code JJY (Multi-Analyte Controls, All Kinds (Assayed)), a Class I device regulated under 21 CFR 862.1660. Techno-Path Manufacturing , Ltd. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 20, 2013
- Date Received
- July 8, 2013
- 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