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FDA 510(k)

CERULOPLASMIN FOR THE TECHNICON DPA-1(TM) SYSTEM

K-Number: K882622 · 1988-07-08

ApplicantTechnicon Instruments Corp.
Decision Date1988-07-08
Product CodeJFR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

CERULOPLASMIN FOR THE TECHNICON DPA-1(TM) SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Instruments Corp.. It received FDA 510(k) clearance on 1988-07-08 under 510(k) number K882622. The device is classified under product code JFR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERULOPLASMIN FOR THE TECHNICON DPA-1(TM) SYSTEM?

CERULOPLASMIN FOR THE TECHNICON DPA-1(TM) SYSTEM is a medical device that received FDA 510(k) clearance on 1988-07-08. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K882622.

When did CERULOPLASMIN FOR THE TECHNICON DPA-1(TM) SYSTEM receive FDA 510(k) clearance?

CERULOPLASMIN FOR THE TECHNICON DPA-1(TM) SYSTEM received FDA 510(k) clearance on 1988-07-08, under 510(k) number K882622.

Who is the listed applicant for CERULOPLASMIN FOR THE TECHNICON DPA-1(TM) SYSTEM?

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

What is the FDA product code for CERULOPLASMIN FOR THE TECHNICON DPA-1(TM) SYSTEM?

The FDA product code for CERULOPLASMIN FOR THE TECHNICON DPA-1(TM) SYSTEM is JFR.

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Other records listing Technicon Instruments Corp. 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.

K914888TECHNICON CHEM 1(TM) SYST (GEN2 SYST)K914511TECHNICON AXON(TM) SYSTEM METHODS ANYALYE HDL CHOLK914025TECHNICON AXON(TM) SYSTEMS, ALT(P 5-P)/AST(P 5-P)K912616TECHNICON IMMUNO 1 TM SYSTEM ADDITIONAL ANALYTESK912413CHEM-LINK DATA BASE MANAGERK903824DRUG OF ABUSE ANALYSIS SYSTEM FREE RADICAL ASSAY

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Related Devices (Code: JFR)

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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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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