3K-CAL Hematology Calibrator/Multiple

FDA 510(k) K912357 · R&D Systems, Inc.

Substantially Equivalent

510(k) numberK912357

Submission

Device name
3K-CAL Hematology Calibrator/Multiple
Applicant
R&D Systems, Inc.
Minneapolis, MN, US
Received
May 28, 1991
Decision date
July 9, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
KRX – Calibrator For Cell Indices
Device class
Class II (moderate risk)
Regulation
21 CFR 864.8150
Specialty
Hematology

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Questions and answers

When was 3K-CAL Hematology Calibrator/Multiple cleared by the FDA?

3K-CAL Hematology Calibrator/Multiple (K912357) received a 510(k) decision of Substantially Equivalent on July 9, 1991, 42 days after the submission was received.

What is the product code of K912357?

The FDA product code is KRX – Calibrator For Cell Indices, a Class II (moderate risk) device regulated under 21 CFR 864.8150.