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)

CEPHALOMETER & FIXATOR

K-Number: K833006 · 1984-01-03

ApplicantModern Systems, Inc.
Decision Date1984-01-03
Product CodeEAG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CEPHALOMETER & FIXATOR is the device name listed in this FDA 510(k) record. The listed applicant is Modern Systems, Inc.. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K833006. The device is classified under product code EAG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEPHALOMETER & FIXATOR?

CEPHALOMETER & FIXATOR is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Modern Systems, Inc.. The 510(k) number is K833006.

When did CEPHALOMETER & FIXATOR receive FDA 510(k) clearance?

CEPHALOMETER & FIXATOR received FDA 510(k) clearance on 1984-01-03, under 510(k) number K833006.

Who is the listed applicant for CEPHALOMETER & FIXATOR?

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

What is the FDA product code for CEPHALOMETER & FIXATOR?

The FDA product code for CEPHALOMETER & FIXATOR is EAG.

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: EAG)

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.

K030699VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRICJ. Morita Mfg. Corp.K021372VERAVIEWEPOCS PANORAMIC X-RAY UNIT WITH CEPHALOMETRIC CAPABILITYJ. Morita USA, Inc.K944162DENAR ACCUCEPH CEPHALOMETER IMAGING SYSTEMTeledyne Water PikK920189GX-C CEPHALOMETERGendex Corp.K896099DIGIGRAPH DIAGNOSTIC WORK/STATIONDolphin Imaging SystemsK870243BURNETT TMJ APPLIANCEMedrad, 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.

↑