510(k) K844947
K844947 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "EMIT ANCILLARY REAGENTS". The FDA issued a decision of Substantially Equivalent on June 28, 1985. The device falls under product code KIE (Apparatus, High Pressure Liquid Chromatography), a Class I device regulated under 21 CFR 862.2260. Syva Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 28, 1985
- Date Received
- December 20, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Apparatus, High Pressure Liquid Chromatography
- Device Class
- Class I
- Regulation Number
- 862.2260
- Review Panel
- TX
- Submission Type