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FDA 510(k)

ASSAY SOFTWARE FOR DPC-MARJ5 ALASTAT EIA SOFTWARE

K-Number: K923879 · 1992-12-07

ApplicantDiagnostic Products Corp.
Decision Date1992-12-07
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ASSAY SOFTWARE FOR DPC-MARJ5 ALASTAT EIA SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Products Corp.. It received FDA 510(k) clearance on 1992-12-07 under 510(k) number K923879. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASSAY SOFTWARE FOR DPC-MARJ5 ALASTAT EIA SOFTWARE?

ASSAY SOFTWARE FOR DPC-MARJ5 ALASTAT EIA SOFTWARE is a medical device that received FDA 510(k) clearance on 1992-12-07. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K923879.

When did ASSAY SOFTWARE FOR DPC-MARJ5 ALASTAT EIA SOFTWARE receive FDA 510(k) clearance?

ASSAY SOFTWARE FOR DPC-MARJ5 ALASTAT EIA SOFTWARE received FDA 510(k) clearance on 1992-12-07, under 510(k) number K923879.

Who is the listed applicant for ASSAY SOFTWARE FOR DPC-MARJ5 ALASTAT EIA SOFTWARE?

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

What is the FDA product code for ASSAY SOFTWARE FOR DPC-MARJ5 ALASTAT EIA SOFTWARE?

The FDA product code for ASSAY SOFTWARE FOR DPC-MARJ5 ALASTAT EIA SOFTWARE is JQW.

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Other records listing Diagnostic Products 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.

K063045IMMULITE 2000, IMMULITE 2500 VANCOMYCINK034055IMMULITE 2500 CK-MB, 2500 MYOGLOBIN, 2500 STAT TROPONIN IK033234IMMULITE 2500 AUTOMATED IMMUNOASSAY ANALYZERK032881IMMULITE/IMMULITE 1000 TOTAL TESTOSTERONE AND IMMULITE 2000 TOTAL TESTOSTERONEK023152IMMULITE 2000 ALLERGEN-SPECIFIC IGEK023304IMMULITE/IMMULITE 1000 CALCITONIN, MODEL LKCL AND IMMULITE 2000 CALCITONIN, MODEL L2KCL

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Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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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