510(k) K935666
K935666 is an FDA 510(k) premarket notification submitted by The Perkin-Elmer Corp. for the device "PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP". The FDA issued a decision of Substantially Equivalent on April 26, 1994. The device falls under product code KIE (Apparatus, High Pressure Liquid Chromatography), a Class I device regulated under 21 CFR 862.2260. The Perkin-Elmer Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 26, 1994
- Date Received
- November 26, 1993
- 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