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FDA 510(k)

COAT-A-COUNT TOTAL IGE IRMA, CATALOG #IKIE1, IKIE2

K-Number: K901859 · 1990-05-03

ApplicantDiagnostic Products Corp.
Decision Date1990-05-03
Product CodeJHR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

COAT-A-COUNT TOTAL IGE IRMA, CATALOG #IKIE1, IKIE2 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 1990-05-03 under 510(k) number K901859. The device is classified under product code JHR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COAT-A-COUNT TOTAL IGE IRMA, CATALOG #IKIE1, IKIE2?

COAT-A-COUNT TOTAL IGE IRMA, CATALOG #IKIE1, IKIE2 is a medical device that received FDA 510(k) clearance on 1990-05-03. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K901859.

When did COAT-A-COUNT TOTAL IGE IRMA, CATALOG #IKIE1, IKIE2 receive FDA 510(k) clearance?

COAT-A-COUNT TOTAL IGE IRMA, CATALOG #IKIE1, IKIE2 received FDA 510(k) clearance on 1990-05-03, under 510(k) number K901859.

Who is the listed applicant for COAT-A-COUNT TOTAL IGE IRMA, CATALOG #IKIE1, IKIE2?

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 COAT-A-COUNT TOTAL IGE IRMA, CATALOG #IKIE1, IKIE2?

The FDA product code for COAT-A-COUNT TOTAL IGE IRMA, CATALOG #IKIE1, IKIE2 is JHR.

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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: JHR)

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.

K061970ELECSYS IGE II IMMUNOASSAYRoche DiagnosticsK984326ELECYS IGE ASSAYBoehringer Mannheim Corp.K960067IMMILITE TOTAL IGEDiagnostic Products Corp.K931703IMMULITE TOTAL IGEDiagnostic Products Corp.K903000TURBO-RAST SPECIFIC IGE ASSAYVentrex Laboratories, Inc.K882616ALTERNATE PROCEDURE, PHARMACIA IGE EIAPharmacia, 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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