Cleared Traditional

K842746 - HYCEL ROTOR-MIXER AND/OR MULTI (FDA 510(k) Clearance)

Aug 1984
Decision
35d
Days
Class 1
Risk

K842746 is an FDA 510(k) clearance for the HYCEL ROTOR-MIXER AND/OR MULTI. This device is classified as a Device, Blood Mixing And Blood Weighing (Class I - General Controls, product code KSQ).

Submitted by R&D Systems, Inc. (Mchenry, US). The FDA issued a Cleared decision on August 17, 1984, 35 days after receiving the submission on July 13, 1984.

This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.9195.

Submission Details

510(k) Number K842746 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 13, 1984
Decision Date August 17, 1984
Days to Decision 35 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary

Device Classification

Product Code KSQ — Device, Blood Mixing And Blood Weighing
Device Class Class I - General Controls
CFR Regulation 21 CFR 864.9195