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FDA 510(k)

DUPONT ACA MAGNESIUM CALIBRATOR

K-Number: K841955 · 1984-06-25

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1984-06-25
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DUPONT ACA MAGNESIUM CALIBRATOR 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 1984-06-25 under 510(k) number K841955. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUPONT ACA MAGNESIUM CALIBRATOR?

DUPONT ACA MAGNESIUM CALIBRATOR is a medical device that received FDA 510(k) clearance on 1984-06-25. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K841955.

When did DUPONT ACA MAGNESIUM CALIBRATOR receive FDA 510(k) clearance?

DUPONT ACA MAGNESIUM CALIBRATOR received FDA 510(k) clearance on 1984-06-25, under 510(k) number K841955.

Who is the listed applicant for DUPONT ACA MAGNESIUM CALIBRATOR?

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 DUPONT ACA MAGNESIUM CALIBRATOR?

The FDA product code for DUPONT ACA MAGNESIUM CALIBRATOR is JIS.

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

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: JIS)

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.

K122126DIRECT LDL/HDL CHOLESTEROL CALIBRATORRandox Laboratories LimitedK061251DIMENSION VISTA TOTAL IRON BINDING CAPACITY CALIBRATORDade Behring, Inc.K060266DIMENSION IRON CALIBRATORDade Behring, Inc.K053104DIMENSION CARDIOPHASE HIGH SENSITIVITY C-REACTIVE PROTEIN CALIBRATORDade Behring, Inc.K032697DIMENSION TOTAL TRIIODOTHYRONINE CALIBRATOR (RC414)Dade Behring, Inc.K032608GONOTEC CALIBRATION SOLUTION 300 MOSMOL/KG FOR OSMOMETERGonotec Gesellschaft Fuer Mess-Und Regeltechnik MB

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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