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FDA 510(k)

RIANEN ANGIOTENSIN I RADIOIMMUNOASSAY KI

K-Number: K850054 · 1985-03-29

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1985-03-29
Product CodeCIB
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIANEN ANGIOTENSIN I RADIOIMMUNOASSAY KI is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1985-03-29 under 510(k) number K850054. The device is classified under product code CIB. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIANEN ANGIOTENSIN I RADIOIMMUNOASSAY KI?

RIANEN ANGIOTENSIN I RADIOIMMUNOASSAY KI is a medical device that received FDA 510(k) clearance on 1985-03-29. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K850054.

When did RIANEN ANGIOTENSIN I RADIOIMMUNOASSAY KI receive FDA 510(k) clearance?

RIANEN ANGIOTENSIN I RADIOIMMUNOASSAY KI received FDA 510(k) clearance on 1985-03-29, under 510(k) number K850054.

Who is the listed applicant for RIANEN ANGIOTENSIN I RADIOIMMUNOASSAY KI?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RIANEN ANGIOTENSIN I RADIOIMMUNOASSAY KI?

The FDA product code for RIANEN ANGIOTENSIN I RADIOIMMUNOASSAY KI is CIB.

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Other records listing E.I. Dupont DE Nemours & Co., Inc. as applicant

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K951851ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAYK953724CRONEX RADIATION THERAPY CASSETTEK953725CRONEX RADIATION THERAPY VERIFICATION CASSETTEK951441DUPONT ACA DIGOXIN (DGN A) METHODK950137URINE BARBITURATES SCREEN FLEX(TM) REAGENT CARTRIDGEK950136URINE OPIATES SCREEN FLEX(TM) REAGENT CARTRIDGE

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Related Devices (Code: CIB)

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.

K123763IDS ISYS DIRECT RENIN ASSAY, IDS ISYS DIRECT RENIN CONTROL SET, AND IDS ISYS DIRECT RENIN CALIBRATION VERIFIERSImmunodiagnostic Systems , Ltd.K121944LIAISON DIRECT RENIN LIAISON CONTROL DIRECT RENIN LIAISON ENDOCRINOLOGY DILUENTDiaSorin, Inc.K062120CISBIO RENIN RIA TESTCis Bio InternationalK061758ACTIVE RENIN IRMADiagnostic Systems Laboratories, Inc.K011128NICHOLS ADVANTAGE DIRECT RENIN (CALIBRATORS, CALIBRATION VERIFIERS, CONTROLS, AND SAMPLE DILUENT)Nichols Institute DiagnosticsK981607ACTIVE RENIN IRMA MODEL NUMBER DSL-25100Diagnostic Systems 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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