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FDA 510(k)

NOVA 13 SODIUM/POTASSIUM/CHLORIDE/LITHIUM ANALYZER

K-Number: K872190 · 1987-06-24

ApplicantNova Biomedical Corp.
Decision Date1987-06-24
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NOVA 13 SODIUM/POTASSIUM/CHLORIDE/LITHIUM ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Nova Biomedical Corp.. It received FDA 510(k) clearance on 1987-06-24 under 510(k) number K872190. The device is classified under product code JGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVA 13 SODIUM/POTASSIUM/CHLORIDE/LITHIUM ANALYZER?

NOVA 13 SODIUM/POTASSIUM/CHLORIDE/LITHIUM ANALYZER is a medical device that received FDA 510(k) clearance on 1987-06-24. The listed applicant is Nova Biomedical Corp.. The 510(k) number is K872190.

When did NOVA 13 SODIUM/POTASSIUM/CHLORIDE/LITHIUM ANALYZER receive FDA 510(k) clearance?

NOVA 13 SODIUM/POTASSIUM/CHLORIDE/LITHIUM ANALYZER received FDA 510(k) clearance on 1987-06-24, under 510(k) number K872190.

Who is the listed applicant for NOVA 13 SODIUM/POTASSIUM/CHLORIDE/LITHIUM ANALYZER?

The FDA 510(k) record lists Nova Biomedical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOVA 13 SODIUM/POTASSIUM/CHLORIDE/LITHIUM ANALYZER?

The FDA product code for NOVA 13 SODIUM/POTASSIUM/CHLORIDE/LITHIUM ANALYZER is JGS.

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Other records listing Nova Biomedical Corp. as applicant

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K100602NOVA STATSTRIP LACTATE HOSPITAL METER, NOVA STATSTRIP LACTATE TEST STRIPSK101633NOVA MAX PLUS GLOCOSE AND B-KETONE CONTROL SOLUTION-MID, HIGHK091547NOVA MAX PLUS BLOOD GLUCOSE AND B-KETONE MONITOR SYSTEM, NOVA MAX PLUS B-KETONE CONTROL SOLUTIONS, NOVA MAX BLOOD GLUCOSK070960NOVA STATSTRIP XPRESS GLUCOSE HOSPITAL METER SYSTEMK070255NOVA MAX BLOOD GLUCOSE MONITOR SYSTEM, 90001,90002K070068NOVA STATSENSOR CREATININE HOSPITAL METER, CONTROL SOLUTIONS,LINEARITY SOLUTIONS, AND TEST STRIPS

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Related Devices (Code: JGS)

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.

K252475ABL90 FLEX PLUS SystemRadiometer Medicals ApsK230275i-STAT CG8+ cartridge with the i-STAT 1 SystemAbbott Point of Care, Inc.K222438A-LYTE® Integrated Multisensor (IMT Na K Cl)Siemens Healthcare Diagnostics, Inc.K220977ISE Reagents, Glucose, CRP Latex, DxC 500 AU Clinical Chemistry AnalyzerBeckman Coulter Laboratory Systems (Suzhou) Co., Ltd.K213486GLP systems TrackAbbott LaboratoriesK200403Stat Profile Prime Plus Analyzer SystemNova Biomedical Corporation

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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