Instrumentation, High Pressure Liquid Chromatography
FDA product code LDM · 19 cleared devices
Class 1
Clinical Chemistry
- Regulation
- 21 CFR 862.2260
- Review panel
- TX
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1978-07-27 – 1996-07-08
LDM
1996-07-08
LDM
1996-07-05
ALLIANCE 2690 SEPARATIONS MODULE
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LDM
1994-11-10
BIO-RAD CLINICAL DATA MANAGEMENT SYSTEM
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LDM
1992-09-11
WATERS(TM) LC MODULE I FOR CLINICAL USE
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LDM
1992-02-19
WATERS 717 AUTOSAMPLER
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LDM
1990-09-11
MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETE
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LDM
1989-02-02
MODEL 250 LIQUID CHROMOTAGRAPHY PUMP
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LDM
1987-07-16
HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM
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LDM
1987-04-22
WATERS 650 ADVANCED PROTEIN PURIFICATION SYSTEM
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LDM
1986-07-14
ISOPURE LC SYSTEM
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LDM
1985-03-06
WATERS 740 DATA MODULE-PLOTTER INTEGRATOR
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LDM
1985-03-05
WATERS 460 LIQUID CHROMATOGRAPHY ELECTROCHEMICAL D
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LDM
1983-11-21
REPORTING INTEGRATOR 3392A
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LDM
1983-10-14
LIQUID CHROMATOGRAPH 1090 SERIES
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LDM
1982-06-22
SERIES 10 LIQUID CHROMOTOGRAPH
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LDM
1982-05-28
SERIES 4 LIQUID CHROMATOGRAPH
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LDM
1981-02-25
MODEL LC-85 UV DETECTOR
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LDM
1980-09-16
3390A REPORTING INTEGRATOR
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LDM
1978-07-27
PREP I AUTOMATED SAMPLE PROCESSOR
View details →No matching devices.
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