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FDA 510(k)

MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING

K-Number: K953477 · 1995-10-07

ApplicantThe DU Pont Co.
Decision Date1995-10-07
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING is the device name listed in this FDA 510(k) record. The listed applicant is The DU Pont Co.. It received FDA 510(k) clearance on 1995-10-07 under 510(k) number K953477. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING?

MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING is a medical device that received FDA 510(k) clearance on 1995-10-07. The listed applicant is The DU Pont Co.. The 510(k) number is K953477.

When did MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING receive FDA 510(k) clearance?

MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING received FDA 510(k) clearance on 1995-10-07, under 510(k) number K953477.

Who is the listed applicant for MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING?

The FDA 510(k) record lists The DU Pont Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING?

The FDA product code for MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING is LMC.

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Other records listing The DU Pont Co. 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.

K953475CDS COMPACT DAYLIGHT CASSETTE FOR VIDEO IMAGINGK952891CRONEX LOW ABSORPTION CASSETTEK945125DUPONT ACA VANCOMYCIN (VANC) METHODK943704LIPASE CALIBRATORK900492LABELING CHANGE - VIASPAN(TM) (BELZER UW)K885259ACA THYRONINE UPTAKE (TU E) METHOD

View all 13 devices →

Related Devices (Code: LMC)

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.

K111566DRYVIEW CHROMA IMAGING SYSTEMCarestream Health, Inc.K092280CYPHER DICOM PRINT SOLUTIONVirtual Imaging, Inc.K090469CARESTREAM DRYVIEW 5850 LASER IMAGERCarestream Health, Inc.K083522SONY UP-DF750 DIGITAL FILM IMAGERSony Electronics, Inc.K081637LASER IMAGER DRYPRO MODEL 873Konica Minolta Medical & Graphic, Inc.K072680DRYSTAR AXYS, MODEL EYZ4EAgfa Healthcare Corporation

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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