Product code LDM— Clinical Chemistry
3390A REPORTING INTEGRATOR
- Classification name
- Instrumentation, High Pressure Liquid Chromatography
- Device class
- Class 1
- Regulation
- 21 CFR 862.2260
- Advisory panel
- Clinical Chemistry
- Total cleared
- 19
- First cleared
- Most recent
Market context for product code LDM
FDA has cleared devices under product code LDM between 1978 and 1996, filed by 6 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1996
- 1994
- 1992
- 1990
- 1989
- 1987
- 1986
- 1985
- 1983
- 1982
- 1981
- 1980
- 1978
Top applicants under product code LDM
Recent clearances under product code LDM
- K960392 — CDM
- K961557 — ALLIANCE 2690 SEPARATIONS MODULE
- K942451 — BIO-RAD CLINICAL DATA MANAGEMENT SYSTEM
- K922388 — WATERS(TM) LC MODULE I FOR CLINICAL USE
- K920136 — WATERS 717 AUTOSAMPLER
- K903647 — MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETE
- K884886 — MODEL 250 LIQUID CHROMOTAGRAPHY PUMP
- K872582 — HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM
- K870949 — WATERS 650 ADVANCED PROTEIN PURIFICATION SYSTEM
- K862178 — ISOPURE LC SYSTEM
- K850272 — WATERS 740 DATA MODULE-PLOTTER INTEGRATOR
- K850359 — WATERS 460 LIQUID CHROMATOGRAPHY ELECTROCHEMICAL D
- K833113 — REPORTING INTEGRATOR 3392A
- K832375 — LIQUID CHROMATOGRAPH 1090 SERIES
- K821727 — SERIES 10 LIQUID CHROMOTOGRAPH
- K821219 — SERIES 4 LIQUID CHROMATOGRAPH
- K810304 — MODEL LC-85 UV DETECTOR
- K802031 — 3390A REPORTING INTEGRATOR
- K780933 — PREP I AUTOMATED SAMPLE PROCESSOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.