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FDA 510(k)

MICRO-HEMATOCRIT CENTRIFUGE 335/336

K-Number: K823558 · 1983-01-21

ApplicantFisher Scientific Co., LLC
Decision Date1983-01-21
Product CodeJPI
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MICRO-HEMATOCRIT CENTRIFUGE 335/336 is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1983-01-21 under 510(k) number K823558. The device is classified under product code JPI. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-HEMATOCRIT CENTRIFUGE 335/336?

MICRO-HEMATOCRIT CENTRIFUGE 335/336 is a medical device that received FDA 510(k) clearance on 1983-01-21. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K823558.

When did MICRO-HEMATOCRIT CENTRIFUGE 335/336 receive FDA 510(k) clearance?

MICRO-HEMATOCRIT CENTRIFUGE 335/336 received FDA 510(k) clearance on 1983-01-21, under 510(k) number K823558.

Who is the listed applicant for MICRO-HEMATOCRIT CENTRIFUGE 335/336?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRO-HEMATOCRIT CENTRIFUGE 335/336?

The FDA product code for MICRO-HEMATOCRIT CENTRIFUGE 335/336 is JPI.

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Other records listing Fisher Scientific Co., LLC as applicant

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K930415MICROHEMATOCRIT ROTORK915825MARATHON 6K GENERAL-PURPOSE CENTRIFUGEK915441MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGEK890534MODIFIED URIQUAL(TM) URINALYSIS CONTROL LEVEL 1K881275URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & IIK874054FISHER DIAGNOSTICS HEMATALL III LAS REAGENT

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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