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FDA 510(k)

DU PONT IDENTIFICATION CAMERA

K-Number: K910354 · 1991-03-29

ApplicantDupont Medical Products
Decision Date1991-03-29
Product CodeJAC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DU PONT IDENTIFICATION CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Dupont Medical Products. It received FDA 510(k) clearance on 1991-03-29 under 510(k) number K910354. The device is classified under product code JAC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DU PONT IDENTIFICATION CAMERA?

DU PONT IDENTIFICATION CAMERA is a medical device that received FDA 510(k) clearance on 1991-03-29. The listed applicant is Dupont Medical Products. The 510(k) number is K910354.

When did DU PONT IDENTIFICATION CAMERA receive FDA 510(k) clearance?

DU PONT IDENTIFICATION CAMERA received FDA 510(k) clearance on 1991-03-29, under 510(k) number K910354.

Who is the listed applicant for DU PONT IDENTIFICATION CAMERA?

The FDA 510(k) record lists Dupont Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DU PONT IDENTIFICATION CAMERA?

The FDA product code for DU PONT IDENTIFICATION CAMERA is JAC.

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Other records listing Dupont Medical Products 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.

K952815DUPONT LIPASE CALIBRATORK950920DUPONT DIMENSION TOTAL PROTEIN METHODK952816LIPASE FLEX REAGENT CARTRIDGEK952412DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROLK945280DUPONT DIMENSION C-REACTIVE PROTEIN METHODK944932PHENOBARBITAL FLEX REAGENT CARTRIDGE

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Related Devices (Code: JAC)

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.

K942883DIGITAL I.D. CAMERAMiles Inc., Agfa DivisionK930752CT/MRI TOPOGRAPHIC MARKERI.Z.I. Corp.K932357FUJI EC ID CAMERAFujifilm Medical System U.S.A., Inc.K925892SOLSTICE XRAY RING MARKER PADSolstice Corp.K926404KODAK X-OMATIC IDENTIFICATION CAMERA, MODEL 4 & 4LEastman Kodak CompanyK923533ADMARKPlanmeca USA, 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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