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FDA 510(k)

AUTOMATED IMMUNOPRECIPITIN METHOD/ICG

K-Number: K803272 · 1981-01-26

ApplicantIcl Scientific
Decision Date1981-01-26
Product CodeDFZ
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

AUTOMATED IMMUNOPRECIPITIN METHOD/ICG is the device name listed in this FDA 510(k) record. The listed applicant is Icl Scientific. It received FDA 510(k) clearance on 1981-01-26 under 510(k) number K803272. The device is classified under product code DFZ. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATED IMMUNOPRECIPITIN METHOD/ICG?

AUTOMATED IMMUNOPRECIPITIN METHOD/ICG is a medical device that received FDA 510(k) clearance on 1981-01-26. The listed applicant is Icl Scientific. The 510(k) number is K803272.

When did AUTOMATED IMMUNOPRECIPITIN METHOD/ICG receive FDA 510(k) clearance?

AUTOMATED IMMUNOPRECIPITIN METHOD/ICG received FDA 510(k) clearance on 1981-01-26, under 510(k) number K803272.

Who is the listed applicant for AUTOMATED IMMUNOPRECIPITIN METHOD/ICG?

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 AUTOMATED IMMUNOPRECIPITIN METHOD/ICG?

The FDA product code for AUTOMATED IMMUNOPRECIPITIN METHOD/ICG is DFZ.

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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: DFZ)

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.

K092283DIMENSION VISTA IMMUNOGLOBULIN IGG SUBCLASSS 1FLEX REAGENT CARTRIDGE, DIMENSION VISTA IMMUNOGLOBULIN IGGSiemens Healthcare DiagnosticsK021081HUMAN IGG SUBCLASS LIQUID REAGENT KITS FOR USE ON THE HITACHI 911/7070 TURBIDIMETRIC ANALYSERThe Binding Site, Ltd.K020823PELICLASS HUMAN IGG SUBCLASS NEPHELOMETRIC IMMAGE KITSanquin Blood Supply FoundationK955906BOEHRINGER MANNHEIM IGG ASSAYBoehringer Mannheim Corp.K940422IGG SUBCLASS SINGLE DILUTION DIAGNOSTIC KIT FOR USE WITH THE BECKMAN ARRAY ANALYZERThe Binding Site, Ltd.K812821H-103 IGG, H-104 IGA, H-105 IGMImmulok, 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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