Cleared Traditional

CAVRO IQ-190 SAMPLE PROCESSOR

K822208 · Cavro Scientific Instruments, Inc. · Chemistry
Aug 1982
Decision
35d
Days
Class 1
Risk

About This 510(k) Submission

K822208 is an FDA 510(k) clearance for the CAVRO IQ-190 SAMPLE PROCESSOR, a Station, Pipetting And Diluting, For Clinical Use (Class I — General Controls, product code JQW), submitted by Cavro Scientific Instruments, Inc. (Walker, US). The FDA issued a Cleared decision on August 27, 1982, 35 days after receiving the submission on July 23, 1982. This device falls under the Chemistry review panel. Regulated under 21 CFR 862.2750.

Submission Details

510(k) Number K822208 FDA.gov
FDA Decision Cleared SESE
Date Received July 23, 1982
Decision Date August 27, 1982
Days to Decision 35 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code JQW — Station, Pipetting And Diluting, For Clinical Use
Device Class Class I — General Controls
CFR Regulation 21 CFR 862.2750

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