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FDA 510(k)

FISHER DIAGNOSTICS HEMATALL III LAS REAGENT

K-Number: K874054 · 1987-10-20

ApplicantFisher Scientific Co., LLC
Decision Date1987-10-20
Product CodeGGK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

FISHER DIAGNOSTICS HEMATALL III LAS REAGENT 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 1987-10-20 under 510(k) number K874054. The device is classified under product code GGK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FISHER DIAGNOSTICS HEMATALL III LAS REAGENT?

FISHER DIAGNOSTICS HEMATALL III LAS REAGENT is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K874054.

When did FISHER DIAGNOSTICS HEMATALL III LAS REAGENT receive FDA 510(k) clearance?

FISHER DIAGNOSTICS HEMATALL III LAS REAGENT received FDA 510(k) clearance on 1987-10-20, under 510(k) number K874054.

Who is the listed applicant for FISHER DIAGNOSTICS HEMATALL III LAS REAGENT?

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 FISHER DIAGNOSTICS HEMATALL III LAS REAGENT?

The FDA product code for FISHER DIAGNOSTICS HEMATALL III LAS REAGENT is GGK.

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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 & IIK872916HISTOMATIC SLIDE STAINER, CODE-ON VERSION

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Related Devices (Code: GGK)

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.

K883836COULTER CLONE QUICK STAIN WHOLE BLOOD LYSE-IICoulter ImmunologyK883991KVM HEMOGLOBIN LYSING REAGENTKvm Technologies, Inc.K873348CELL-DYN DIFF SCREEN, AUTO. & SEMI AUTO. LYTIC AG.Abbott DiagnosticsK863114PIASTRINITJ. D. Assoc.K863503HEMOLYSEReagent Laboratory, Inc.K850097LASER-LYSEHematology Marketing Assoc.

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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