Calibrator 282

FDA 510(k) K831872 · Bionostics, Inc.

Substantially Equivalent

510(k) numberK831872

Submission

Device name
Calibrator 282
Applicant
Bionostics, Inc.
Mchenry, IL, US
Received
June 13, 1983
Decision date
July 18, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KRZ – Calibrator For Hemoglobin And Hematocrit Measurement
Device class
Class II (moderate risk)
Regulation
21 CFR 864.8165
Specialty
Hematology

Other 510(k)s with product code KRZ

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K052101C.F.A.S. (Calibrator for Automated Systems) HBA1CKRZ · Abbreviated Roche Diagnostics08/26/2005SE
K041130CDS Hematology Calibrator (CDS Cal)KRZ · Abbreviated Clinical Diagnostic Solutions, Inc.06/10/2004SE
K962864THB Cal Standard for Il Co-Oximeters/OximetersKRZ · Traditional Alko Diagnostic Corp.12/18/1996SE
K951071Alko Slope THB Solution for Corning 280, 288 and 2500 AnalyzersKRZ · Traditional Alko Diagnostic Corp.07/24/1995SE
K902892Cell-Dyn CalibratorKRZ · Traditional Unipath , Ltd.09/10/1990SE
K896921Raichem TM Hemoglobin CalibratorKRZ · Traditional Reagents Applications, Inc.01/25/1990SE
K893984Hgb-Cal Set/MultipleKRZ · Traditional R&D Systems, Inc.08/15/1989SE
K883851Msi-Cal 8KRZ · Traditional Medical Specialties, Inc.11/22/1988SE
K883850Msi-Cal 16KRZ · Traditional Medical Specialties, Inc.11/22/1988SE
K883703Msi-Cal 7KRZ · Traditional Medical Specialties, Inc.11/22/1988SE

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Questions and answers

When was Calibrator 282 cleared by the FDA?

Calibrator 282 (K831872) received a 510(k) decision of Substantially Equivalent on July 18, 1983, 35 days after the submission was received.

What is the product code of K831872?

The FDA product code is KRZ – Calibrator For Hemoglobin And Hematocrit Measurement, a Class II (moderate risk) device regulated under 21 CFR 864.8165.