Product code KZR— Clinical Chemistry
2487 DUAL WAVELENGTH ABSORBANCE DETECTOR
- Classification name
- Chromatography (Liquid, Gel), Clinical Use
- Device class
- Class 1
- Regulation
- 21 CFR 862.2260
- Advisory panel
- Clinical Chemistry
- Total cleared
- 15
- First cleared
- Most recent
Market context for product code KZR
FDA has cleared devices under product code KZR between 1977 and 1997, filed by 8 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
- 1997
- 1993
- 1991
- 1986
- 1985
- 1984
- 1983
- 1980
- 1978
- 1977
Top applicants under product code KZR
Recent clearances under product code KZR
- K973074 — 2487 DUAL WAVELENGTH ABSORBANCE DETECTOR
- K931227 — USDT FLOW IMMUNOASSAY SYSTEM, MODEL 9000
- K905538 — COLUMNS LIQUID CHROMATOGRAPHY DPM
- K861392 — SYVA SOLID PHASE COLUMNS SYSTEM II
- K860197 — SERIES 410 LC PUMP
- K851945 — VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM
- K843568 — LIQUID CHROMATOGRAPH 400
- K841890 — VARIAN 2000 LIQUID CHROMATOGRAPHY ANALY
- K840977 — LIQUID CHROMATOGRAPHIC DETECTOR LC-95
- K832201 — CHROM-PREP
- K802725 — VISTA 54 LIQUID CHROMATOGRAPHY ANAL. SYS
- K780944 — LIQUID CHROMATOGRAPH MODEL 850
- K780945 — LIQUID CHROMATOGRAPH MODEL 860
- K770255 — LC-65T DETECTOR AND OVEN
- K770254 — CHROMATOGRAPH, SERIES 3, LIQUID
Data sourced from openFDA. This site is unofficial and independent of the FDA.