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)

SONIA-SO NOGRAPH-NUMERICAL ANALYSIS

K-Number: K801844 · 1980-10-03

ApplicantCgr Medical Corp.
Decision Date1980-10-03
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONIA-SO NOGRAPH-NUMERICAL ANALYSIS is the device name listed in this FDA 510(k) record. The listed applicant is Cgr Medical Corp.. It received FDA 510(k) clearance on 1980-10-03 under 510(k) number K801844. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONIA-SO NOGRAPH-NUMERICAL ANALYSIS?

SONIA-SO NOGRAPH-NUMERICAL ANALYSIS is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is Cgr Medical Corp.. The 510(k) number is K801844.

When did SONIA-SO NOGRAPH-NUMERICAL ANALYSIS receive FDA 510(k) clearance?

SONIA-SO NOGRAPH-NUMERICAL ANALYSIS received FDA 510(k) clearance on 1980-10-03, under 510(k) number K801844.

Who is the listed applicant for SONIA-SO NOGRAPH-NUMERICAL ANALYSIS?

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

What is the FDA product code for SONIA-SO NOGRAPH-NUMERICAL ANALYSIS?

The FDA product code for SONIA-SO NOGRAPH-NUMERICAL ANALYSIS is IYO.

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 Cgr Medical Corp. 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.

K843926PRESTILIX 1690K843235STENOSCOPK843985SUSPENSION 7K841649MAXIMAX - 4K833223SONEL 3000AK833941ORION

View all 20 devices →

Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, 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.

↑