Cleared Traditional

HEMOGLOBIN CONTROL LEVELS

K801268 · Bioscientific · Hematology
Jul 1980
Decision
47d
Days
Class 2
Risk

About This 510(k) Submission

K801268 is an FDA 510(k) clearance for the HEMOGLOBIN CONTROL LEVELS, a Whole Blood Hemoglobin Determination (Class II — Special Controls, product code KHG), submitted by Bioscientific (Mchenry, US). The FDA issued a Cleared decision on July 14, 1980, 47 days after receiving the submission on May 28, 1980. This device falls under the Hematology review panel. Regulated under 21 CFR 864.7500.

Submission Details

510(k) Number K801268 FDA.gov
FDA Decision Cleared SESE
Date Received May 28, 1980
Decision Date July 14, 1980
Days to Decision 47 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary —

Device Classification

Product Code KHG — Whole Blood Hemoglobin Determination
Device Class Class II — Special Controls
CFR Regulation 21 CFR 864.7500

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