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FDA 510(k)

LISS REAGENT

K-Number: K790498 · 1979-04-03

ApplicantFisher Scientific Co., LLC
Decision Date1979-04-03
Product CodeKSG
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LISS 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 1979-04-03 under 510(k) number K790498. The device is classified under product code KSG. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LISS REAGENT?

LISS REAGENT is a medical device that received FDA 510(k) clearance on 1979-04-03. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K790498.

When did LISS REAGENT receive FDA 510(k) clearance?

LISS REAGENT received FDA 510(k) clearance on 1979-04-03, under 510(k) number K790498.

Who is the listed applicant for LISS 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 LISS REAGENT?

The FDA product code for LISS REAGENT is KSG.

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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: KSG)

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.

K812565ELUTION SOLUTIONBiological Corp. of AmericaK812222EM-XBiological Corp. of AmericaK800943PENTEX BOVINE ALBUMIN 30% SOLUTIONMiles Laboratories, Inc.K800189BOVINE ALBUMIN 22% & 30% SOLUTIONSGotham Biologics, Inc.K791791ORTHO ANTIBODY ENHANCEMENT SOLUTIONOrtho Diagnostics, Inc.K791113LOW IONIC STRENGTH SOLUTION (LISS)Hyland Therapeutic Div., Travenol Laboratories

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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