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FDA 510(k)

MULTIANALYTE CONTROLS-ALL KINDS

K-Number: K823929 · 1983-01-28

ApplicantFisher Scientific Co., LLC
Decision Date1983-01-28
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MULTIANALYTE CONTROLS-ALL KINDS 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 1983-01-28 under 510(k) number K823929. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIANALYTE CONTROLS-ALL KINDS?

MULTIANALYTE CONTROLS-ALL KINDS is a medical device that received FDA 510(k) clearance on 1983-01-28. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K823929.

When did MULTIANALYTE CONTROLS-ALL KINDS receive FDA 510(k) clearance?

MULTIANALYTE CONTROLS-ALL KINDS received FDA 510(k) clearance on 1983-01-28, under 510(k) number K823929.

Who is the listed applicant for MULTIANALYTE CONTROLS-ALL KINDS?

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 MULTIANALYTE CONTROLS-ALL KINDS?

The FDA product code for MULTIANALYTE CONTROLS-ALL KINDS is JJY.

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Other records listing Fisher Scientific Co., LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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Related Devices (Code: JJY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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