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FDA 510(k)

CIC-C1Q EIA

K-Number: K012576 · 2002-01-29

ApplicantAmerican Laboratory Products Co., Ltd.
Decision Date2002-01-29
Product CodeDAK
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

CIC-C1Q EIA is the device name listed in this FDA 510(k) record. The listed applicant is American Laboratory Products Co., Ltd.. It received FDA 510(k) clearance on 2002-01-29 under 510(k) number K012576. 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 CIC-C1Q EIA?

CIC-C1Q EIA is a medical device that received FDA 510(k) clearance on 2002-01-29. The listed applicant is American Laboratory Products Co., Ltd.. The 510(k) number is K012576.

When did CIC-C1Q EIA receive FDA 510(k) clearance?

CIC-C1Q EIA received FDA 510(k) clearance on 2002-01-29, under 510(k) number K012576.

Who is the listed applicant for CIC-C1Q EIA?

The FDA 510(k) record lists American Laboratory Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CIC-C1Q EIA?

The FDA product code for CIC-C1Q EIA is DAK.

Other records listing American Laboratory Products Co., Ltd. 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.

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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 GmbHK973203THYMOSTAT 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.K914388C1 RID KITThe Binding Site, Ltd.

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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