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 |