Product code JQT— Clinical Chemistry
710 FLUOROMETER/DENSITOMETER
- Classification name
- Densitometer/Scanner (Integrating, Reflectance, Tlc, Radiochromat.) Clinica
- Device class
- Class 1
- Regulation
- 21 CFR 862.2400
- Advisory panel
- Clinical Chemistry
- Total cleared
- 18
- First cleared
- Most recent
Market context for product code JQT
FDA has cleared devices under product code JQT between 1977 and 2011, filed by 13 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
- 2011
- 1994
- 1992
- 1989
- 1986
- 1985
- 1984
- 1981
- 1978
- 1977
Top applicants under product code JQT
Recent clearances under product code JQT
- K111356 — ASIMANAGER - AT
- K944185 — ISOSCAN
- K915332 — MODEL 795 FLUOROMETER/DENSITOMETER
- K885254 — TARGET READER
- K860645 — ELECTROPHORESIS DATA CENTER (EDC)
- K862956 — ICON READER
- K853734 — APOLLO DENSITOMETER
- K851154 — ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18
- K850617 — CORNING 780 FLUOROMETER/DENSITOMETER
- K850260 — GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER
- K842313 — ELVI 146 SEROSCAN
- K842056 — ELVI 165 PROTEO SEROSKOP
- K810619 — 710 FLUOROMETER/DENSITOMETER
- K803240 — CORNING 760 FLUOROMETER/DENSITOMETER
- K780901 — AUTOMATED ELECTROPHORESIS SYSTEM
- K780318 — MODULAR SCANNING DENSITOMETER SYS.
- K772325 — DENSITOMETER 18, COMPUTING, AUTO.
- K770026 — FLOUROMETER/DENSITOMETER MODEL 720
Data sourced from openFDA. This site is unofficial and independent of the FDA.