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FDA 510(k)

CRONEX QC-1 PROCESSOR

K-Number: K780248 · 1978-03-02

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1978-03-02
Product CodeIXW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CRONEX QC-1 PROCESSOR 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 1978-03-02 under 510(k) number K780248. The device is classified under product code IXW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRONEX QC-1 PROCESSOR?

CRONEX QC-1 PROCESSOR is a medical device that received FDA 510(k) clearance on 1978-03-02. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K780248.

When did CRONEX QC-1 PROCESSOR receive FDA 510(k) clearance?

CRONEX QC-1 PROCESSOR received FDA 510(k) clearance on 1978-03-02, under 510(k) number K780248.

Who is the listed applicant for CRONEX QC-1 PROCESSOR?

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 CRONEX QC-1 PROCESSOR?

The FDA product code for CRONEX QC-1 PROCESSOR is IXW.

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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

View all 253 devices →

Related Devices (Code: IXW)

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.

K111167XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER MODEL SPRINTVelopex International, Inc.K093503INTRAX FILM PROCESSORVelopex International, Inc.K091628OPTIMAX, COMPACT 2, OPTIMAX 2010, ECOMAXProtec GmbH & Co. KGK024342RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000Daito Co., Ltd.K023801FILM PROCESSOR, MODEL LIFE RAY PRO 1000S.A.I.E.P. S.R.L.K023825FILM PROCESSOR, MODEL LIFE RAY PRO 2500S.A.I.E.P. S.R.L.

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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