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

FDA 510(k)

I-Q View

K-Number: K203703 · 2021-03-24

ApplicantFirst Source, Inc.
Decision Date2021-03-24
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

I-Q View is a medical device manufactured by First Source, Inc.. It received FDA 510(k) clearance on 2021-03-24 under approval number K203703. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I-Q View?

I-Q View is a medical device that received FDA 510(k) clearance on 2021-03-24. It is manufactured by First Source, Inc.. The 510(k) number is K203703.

When was I-Q View approved by the FDA?

I-Q View received FDA 510(k) clearance on 2021-03-24, under approval number K203703.

What company makes I-Q View?

I-Q View is manufactured by First Source, Inc..

What is the FDA product code for I-Q View?

The FDA product code for I-Q View is MQB.

Other Devices by First Source, Inc.

K221081iQFlex M Mobile X-ray System, iQFlex MD Mobile X-ray System K240009iQFlex Pro

Related Devices (Code: MQB)

K162555EVS 4343, EVS 4343GDRTECH Corporation K162344INNOLUX RICInnolux Corporation K161730Wireless Digital Flat Panel DetectorIray Technology (Shanghai) , Ltd. K162552EVS 3643, EVS 3643GDRTECH Corporation K163019CareView 750Cw/750C X-ray Flat Panel DetectorsCareray Digital Medical System Co., Ltd. K160143ClearVision ExamVue Flat Panel DetectorJpi Healthcare, 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.

↑