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FDA 510(k)

ELECTRO-IMMUNO-QUANTITATION (EIQ)

K-Number: K792472 · 1979-12-27

ApplicantIcl Scientific
Decision Date1979-12-27
Product CodeDAK
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ELECTRO-IMMUNO-QUANTITATION (EIQ) is the device name listed in this FDA 510(k) record. The listed applicant is Icl Scientific. It received FDA 510(k) clearance on 1979-12-27 under 510(k) number K792472. The device is classified under product code DAK. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO-IMMUNO-QUANTITATION (EIQ)?

ELECTRO-IMMUNO-QUANTITATION (EIQ) is a medical device that received FDA 510(k) clearance on 1979-12-27. The listed applicant is Icl Scientific. The 510(k) number is K792472.

When did ELECTRO-IMMUNO-QUANTITATION (EIQ) receive FDA 510(k) clearance?

ELECTRO-IMMUNO-QUANTITATION (EIQ) received FDA 510(k) clearance on 1979-12-27, under 510(k) number K792472.

Who is the listed applicant for ELECTRO-IMMUNO-QUANTITATION (EIQ)?

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

What is the FDA product code for ELECTRO-IMMUNO-QUANTITATION (EIQ)?

The FDA product code for ELECTRO-IMMUNO-QUANTITATION (EIQ) is DAK.

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Other records listing Icl Scientific as applicant

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Related Devices (Code: DAK)

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.

K031563BINDAZYME CLQ CIC EIA KITThe Binding Site, Ltd.K032254IBL C1Q-CIC CIA TESTIbl GmbHK012576CIC-C1Q EIAAmerican Laboratory Products Co., Ltd.K973203THYMOSTAT ELISA FOR THE DETECTION OF HUMAN IGG,M AND A ANTI-RABBIT IGG ANTIBODIESSangstat Medical Corp.K972873IMMUSTRIP HAMA IGGImmunomedics, Inc.K951968HUMAN C1Q RADIAL IMMUNODIFFUSION KITKent Laboratories, 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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