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)

VOLUMETRIC PACKAGE STEPPER H4222AA/CALCU. H4222AB

K-Number: K872307 · 1987-09-08

ApplicantGeneral Electric Co.
Decision Date1987-09-08
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VOLUMETRIC PACKAGE STEPPER H4222AA/CALCU. H4222AB is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1987-09-08 under 510(k) number K872307. 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 VOLUMETRIC PACKAGE STEPPER H4222AA/CALCU. H4222AB?

VOLUMETRIC PACKAGE STEPPER H4222AA/CALCU. H4222AB is a medical device that received FDA 510(k) clearance on 1987-09-08. The listed applicant is General Electric Co.. The 510(k) number is K872307.

When did VOLUMETRIC PACKAGE STEPPER H4222AA/CALCU. H4222AB receive FDA 510(k) clearance?

VOLUMETRIC PACKAGE STEPPER H4222AA/CALCU. H4222AB received FDA 510(k) clearance on 1987-09-08, under 510(k) number K872307.

Who is the listed applicant for VOLUMETRIC PACKAGE STEPPER H4222AA/CALCU. H4222AB?

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

What is the FDA product code for VOLUMETRIC PACKAGE STEPPER H4222AA/CALCU. H4222AB?

The FDA product code for VOLUMETRIC PACKAGE STEPPER H4222AA/CALCU. H4222AB 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 General Electric Co. 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.

K103489GE VEO RECONSTRUCTION OPTIONK082317GE LUNAR FRAX 10-YEAR FRACTURE RISK SOFTWARE OPTIONK081921GE VIVID E9 ULTRASOUNDK073297GE LOGIQ P6K072952GE ECHOPACK072797GE LOGIQ I COMAPACT ULTRASOUND, GE LOGIQ E COMPACT ULTRASOUND, GE VIVID E COMPACT ULTRASOUND

View all 254 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.

↑