The following data is part of a premarket notification filed by The Perkin-elmer Corp. with the FDA for Perkin-elmer Series 200 Liq Chromatographic Pump.
Device ID | K935666 |
510k Number | K935666 |
Device Name: | PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMP |
Classification | Apparatus, High Pressure Liquid Chromatography |
Applicant | THE PERKIN-ELMER CORP. 761 MAIN AVE. Norwalk, CT 06859 |
Contact | John Kent |
Correspondent | John Kent THE PERKIN-ELMER CORP. 761 MAIN AVE. Norwalk, CT 06859 |
Product Code | KIE |
CFR Regulation Number | 862.2260 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-11-26 |
Decision Date | 1994-04-26 |