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FDA 510(k), K861194, ULTROSPEC K KINETICS SPECTROPHOTOMETER
FDA 510(k), K861194, ULTROSPEC K KINETICS SPECTROPHOTOMETER
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510(K) Number: K861194
Device Name: ULTROSPEC K KINETICS SPECTROPHOTOMETER
Manufacturer: LKB INSTRUMENTS, INC.
Device Classification Name: colorimeter, photometer, spectrophotometer for clinical use
Regulation Number: 862.2300
Classification Product Code: JJQ
Date Received: 03/31/1986
Decision Date: 04/24/1986
Regulation Medical Specialty: Clinical Chemistry
Device Name: ULTROSPEC K KINETICS SPECTROPHOTOMETER
Manufacturer: LKB INSTRUMENTS, INC.
Device Classification Name: colorimeter, photometer, spectrophotometer for clinical use
Regulation Number: 862.2300
Classification Product Code: JJQ
Date Received: 03/31/1986
Decision Date: 04/24/1986
Regulation Medical Specialty: Clinical Chemistry
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