KIE · Class I · 21 CFR 862.2260

FDA Product Code KIE: Apparatus, High Pressure Liquid Chromatography

Leading manufacturers include Hewlett-Packard Co., Syva Co. and E.I. Dupont DE Nemours & Co., Inc..

25
Total
25
Cleared
49d
Avg days
1977
Since

FDA 510(k) Cleared Apparatus, High Pressure Liquid Chromatography Devices (Product Code KIE)

25 devices
1–24 of 25
Cleared Jun 28, 1985
EMIT ANCILLARY REAGENTS
K844947
Syva Co.
Toxicology · 190d
Cleared Feb 15, 1985
SYVA SAMPLE SEAL
K844949
Syva Co.
Toxicology · 57d
Cleared Mar 25, 1980
DIFFERENTIAL REFRACTIVE INDEX DETECTOR
K800556
Hewlett-Packard Co.
Toxicology · 13d
Cleared Mar 19, 1980
DUPONT INSTRUMENTS MODEL 870 LIQ. CHROM.
K800516
E.I. Dupont DE Nemours & Co., Inc.
Toxicology · 14d
Cleared Dec 20, 1978
DETECTOR, MODEL 79875A, VARIABLE
K781771
Hewlett-Packard Co.
Toxicology · 68d
Cleared Jan 05, 1978
AUTO. SAMPLING SYSTEM
K772364
Hewlett-Packard Co.
Toxicology · 9d
Cleared Feb 02, 1977
L080 SERIES LIQUID CHROMATOGRAPH
K761351
Hewlett-Packard Co.
Toxicology · 36d

About Product Code KIE - Regulatory Context