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)

ANGIOTEC SC 1221 SCAN CONVERTER

K-Number: K850330 · 1985-04-30

ApplicantAngiotec
Decision Date1985-04-30
Product CodeLMA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ANGIOTEC SC 1221 SCAN CONVERTER is the device name listed in this FDA 510(k) record. The listed applicant is Angiotec. It received FDA 510(k) clearance on 1985-04-30 under 510(k) number K850330. The device is classified under product code LMA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOTEC SC 1221 SCAN CONVERTER?

ANGIOTEC SC 1221 SCAN CONVERTER is a medical device that received FDA 510(k) clearance on 1985-04-30. The listed applicant is Angiotec. The 510(k) number is K850330.

When did ANGIOTEC SC 1221 SCAN CONVERTER receive FDA 510(k) clearance?

ANGIOTEC SC 1221 SCAN CONVERTER received FDA 510(k) clearance on 1985-04-30, under 510(k) number K850330.

Who is the listed applicant for ANGIOTEC SC 1221 SCAN CONVERTER?

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

What is the FDA product code for ANGIOTEC SC 1221 SCAN CONVERTER?

The FDA product code for ANGIOTEC SC 1221 SCAN CONVERTER is LMA.

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

Related Devices (Code: LMA)

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.

K132183DICOM VIDEOBar Code Computer, Ltd.K130636TELERADPRO EDGE; TELERADPRO EDGE HD-CCDVidar Systems Corp.K130406DIAGNOSTICPRO EDGEVidar Systems Corp.K102476TELERADPROVidar Systems Corp.K093809VIDAR DENTAL FILM DIGITIZERVidar Systems Corp.K091288MEDI-6000 MEDICAL IMAGE DIGITIZERMicrotek International, 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.

↑