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FDA 510(k)

SPECIFIC CHEMISTRY ANALYZER

K-Number: K882081 · 1988-07-01

ApplicantThe Rupp & Bowman Co.
Decision Date1988-07-01
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SPECIFIC CHEMISTRY ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is The Rupp & Bowman Co.. It received FDA 510(k) clearance on 1988-07-01 under 510(k) number K882081. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECIFIC CHEMISTRY ANALYZER?

SPECIFIC CHEMISTRY ANALYZER is a medical device that received FDA 510(k) clearance on 1988-07-01. The listed applicant is The Rupp & Bowman Co.. The 510(k) number is K882081.

When did SPECIFIC CHEMISTRY ANALYZER receive FDA 510(k) clearance?

SPECIFIC CHEMISTRY ANALYZER received FDA 510(k) clearance on 1988-07-01, under 510(k) number K882081.

Who is the listed applicant for SPECIFIC CHEMISTRY ANALYZER?

The FDA 510(k) record lists The Rupp & Bowman Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECIFIC CHEMISTRY ANALYZER?

The FDA product code for SPECIFIC CHEMISTRY ANALYZER is JJE.

Related Clinical Trials

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.

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Other records listing The Rupp & Bowman Co. 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.

K880973MICROLYTE 7K880242KONE CALCIUM TEST

Related Devices (Code: JJE)

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.

K183375Yumizen C1200, Yumizen C1200 Glucose HK, Sodium Electrode, Potassium Electrode, Chloride ElectrodeHoriba, Ltd.K130276DIMENSION EXL WITH LM SYSTEMSiemens Healthcare Diagnostics, Inc.K113253ACE AXCEL CLINICAL CHEMISTRY SYSTEM,ACE ALBUMIN REAGENT,ACE TOTAL PROTEIN REAGENT,ACE BUN/UREANITROGEN REAGENTAlfa Wassermann Diagnostic Technologies, Inc.K112999DIMENSION CLINICAL CHEMISTRY SYSTEMSiemens Healthcare DiagnosticsK110035INDIKOThermofisher Scientific OYK073370TC MATRIX CLINICAL CHEMISTRY ANALYZERTeco Diagnostics

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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