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FDA 510(k)

DIGITAL I.D. CAMERA

K-Number: K942883 · 1994-09-30

ApplicantMiles Inc., Agfa Division
Decision Date1994-09-30
Product CodeJAC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL I.D. CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Miles Inc., Agfa Division. It received FDA 510(k) clearance on 1994-09-30 under 510(k) number K942883. 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 DIGITAL I.D. CAMERA?

DIGITAL I.D. CAMERA is a medical device that received FDA 510(k) clearance on 1994-09-30. The listed applicant is Miles Inc., Agfa Division. The 510(k) number is K942883.

When did DIGITAL I.D. CAMERA receive FDA 510(k) clearance?

DIGITAL I.D. CAMERA received FDA 510(k) clearance on 1994-09-30, under 510(k) number K942883.

Who is the listed applicant for DIGITAL I.D. CAMERA?

The FDA 510(k) record lists Miles Inc., Agfa Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL I.D. CAMERA?

The FDA product code for DIGITAL I.D. CAMERA is JAC.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Miles Inc., Agfa Division 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.

K943602DI-2000

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.

K930752CT/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.K925332BENNETT X-RAY ID PLUSBennett X-Ray Technologies

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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