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FDA 510(k)

ANTI-HUMAN CIQ SERUM

K-Number: K781022 · 1978-08-14

ApplicantIcl Scientific
Decision Date1978-08-14
Product CodeDAK
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ANTI-HUMAN CIQ SERUM is the device name listed in this FDA 510(k) record. The listed applicant is Icl Scientific. It received FDA 510(k) clearance on 1978-08-14 under 510(k) number K781022. 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 ANTI-HUMAN CIQ SERUM?

ANTI-HUMAN CIQ SERUM is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Icl Scientific. The 510(k) number is K781022.

When did ANTI-HUMAN CIQ SERUM receive FDA 510(k) clearance?

ANTI-HUMAN CIQ SERUM received FDA 510(k) clearance on 1978-08-14, under 510(k) number K781022.

Who is the listed applicant for ANTI-HUMAN CIQ SERUM?

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 ANTI-HUMAN CIQ SERUM?

The FDA product code for ANTI-HUMAN CIQ SERUM is DAK.

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Other records listing Icl Scientific 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.

K883942HYCOR SENTRY DRUGS OF ABUSE URINE CONTROLK843565KOVA TROL I,II, III HUMAN URINE-DRIEDK833761THERAPEUTIC DRUG CONTROLK832823ENZYMUNE-TEST TSHK831383EVENT-TEST SLIDEK823199ENZYME-TEST DIGOXIN

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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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