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FDA 510(k)

REAGENTS CORNING CHLORIDE METER FOR

K-Number: K830217 · 1983-02-18

ApplicantFisher Scientific Co., LLC
Decision Date1983-02-18
Product CodeJFS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

REAGENTS CORNING CHLORIDE METER FOR 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 1983-02-18 under 510(k) number K830217. The device is classified under product code JFS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAGENTS CORNING CHLORIDE METER FOR?

REAGENTS CORNING CHLORIDE METER FOR is a medical device that received FDA 510(k) clearance on 1983-02-18. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K830217.

When did REAGENTS CORNING CHLORIDE METER FOR receive FDA 510(k) clearance?

REAGENTS CORNING CHLORIDE METER FOR received FDA 510(k) clearance on 1983-02-18, under 510(k) number K830217.

Who is the listed applicant for REAGENTS CORNING CHLORIDE METER FOR?

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 REAGENTS CORNING CHLORIDE METER FOR?

The FDA product code for REAGENTS CORNING CHLORIDE METER FOR is JFS.

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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: JFS)

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.

K121823CLINICAL CHLORIDE ANALYZER, CHLORIDE TEST SYSTEM, SWEAT CHLORIDE ANALYZER, CHLORIDOMETER, CHLORIDE COULOMETRICWescor, Inc.K923598REDI-CHECK PHOTMETER Q.A.Awareness Technology, Inc.K873127CHLORIDE REAGENT KITA-Kem, Inc.K823106RERMCO TEST CHLORIDE REAGENTFermco Biochemics, Inc.K820411LIQUIZYME CHLORIDE REAGENTAmerican Research Products Co.K811319CHLORIDE REAGENT KITChem-Elec, Inc.

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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