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FDA 510(k)

CORNING 902 SODIUM POTASSIUM ANALYZER

K-Number: K820629 · 1982-03-25

ApplicantCorning Medical & Scientific
Decision Date1982-03-25
Product CodeCFM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CORNING 902 SODIUM POTASSIUM ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Corning Medical & Scientific. It received FDA 510(k) clearance on 1982-03-25 under 510(k) number K820629. The device is classified under product code CFM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORNING 902 SODIUM POTASSIUM ANALYZER?

CORNING 902 SODIUM POTASSIUM ANALYZER is a medical device that received FDA 510(k) clearance on 1982-03-25. The listed applicant is Corning Medical & Scientific. The 510(k) number is K820629.

When did CORNING 902 SODIUM POTASSIUM ANALYZER receive FDA 510(k) clearance?

CORNING 902 SODIUM POTASSIUM ANALYZER received FDA 510(k) clearance on 1982-03-25, under 510(k) number K820629.

Who is the listed applicant for CORNING 902 SODIUM POTASSIUM ANALYZER?

The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORNING 902 SODIUM POTASSIUM ANALYZER?

The FDA product code for CORNING 902 SODIUM POTASSIUM ANALYZER is CFM.

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Other records listing Corning Medical & Scientific 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.

K875122DISPOSABLE STERILE SYRINGE FILTERSK872273CORNING EASY WASH ELISA PLATESK872076CORNING DISPOSABLE ROLLER BOTTLESK863789CORNING ELISA PLATESK854024CORNING MAGIC MAB HCG RADIOIMMUNOASSAYK853634CORNING CELL WELLS-MULTIPLE WELL PLATES

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Related Devices (Code: CFM)

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.

K984119WAKO L-TYPE FE, WAKO L-TYPE CALIBRATORWako Chemicals USA, Inc.K981581IRONAbbott LaboratoriesK932871UIBC FOR DISCREET RANDOM ACCESS ANALYZERCatachem, Inc.K913705ABBOTT QLUICKSTART IRON TEST, ITEM #5A29Em Diagnostic Systems, Inc.K912912SYNERMED SERUM IRON-600 REAGENT KITSynermed, Inc.K902918SYNERMED SERUM IRON REAGENT KITSynermed, 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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