Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

5000/5000C MULTI-FORMAT CAMERAS FOR NUCLEAR MEDI.

K-Number: K900897 · 1990-04-19

ApplicantInternational Imaging Electronics
Decision Date1990-04-19
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

5000/5000C MULTI-FORMAT CAMERAS FOR NUCLEAR MEDI. is the device name listed in this FDA 510(k) record. The listed applicant is International Imaging Electronics. It received FDA 510(k) clearance on 1990-04-19 under 510(k) number K900897. 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 5000/5000C MULTI-FORMAT CAMERAS FOR NUCLEAR MEDI.?

5000/5000C MULTI-FORMAT CAMERAS FOR NUCLEAR MEDI. is a medical device that received FDA 510(k) clearance on 1990-04-19. The listed applicant is International Imaging Electronics. The 510(k) number is K900897.

When did 5000/5000C MULTI-FORMAT CAMERAS FOR NUCLEAR MEDI. receive FDA 510(k) clearance?

5000/5000C MULTI-FORMAT CAMERAS FOR NUCLEAR MEDI. received FDA 510(k) clearance on 1990-04-19, under 510(k) number K900897.

Who is the listed applicant for 5000/5000C MULTI-FORMAT CAMERAS FOR NUCLEAR MEDI.?

The FDA 510(k) record lists International Imaging Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 5000/5000C MULTI-FORMAT CAMERAS FOR NUCLEAR MEDI.?

The FDA product code for 5000/5000C MULTI-FORMAT CAMERAS FOR NUCLEAR MEDI. is LMC.

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 International Imaging Electronics 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.

K972019PEFECT SHOTK970964MAESTRO DIGITAL IMAGE AND PATIENT RECORD STORAGE SYSTEMK950330DIGITAL IMAGE ACQUISITION SYSTEMK953165ULTRA COMPACT VIDEO IMAGERK940332MODEL FORTY ULTRA COMPACT VIDEO IMAGERK934908FULL VIEW DIGITAL STORAGE SYSTEM

View all 19 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.

↑