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)

Medical image processing software

K-Number: K220910 · 2022-08-11

Decision Date2022-08-11
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Medical image processing software is a medical device manufactured by Hangzhou Deepwise & League of PHD Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-08-11 under approval number K220910. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medical image processing software?

Medical image processing software is a medical device that received FDA 510(k) clearance on 2022-08-11. It is manufactured by Hangzhou Deepwise & League of PHD Technology Co., Ltd.. The 510(k) number is K220910.

When was Medical image processing software approved by the FDA?

Medical image processing software received FDA 510(k) clearance on 2022-08-11, under approval number K220910.

What company makes Medical image processing software?

Medical image processing software is manufactured by Hangzhou Deepwise & League of PHD Technology Co., Ltd..

What is the FDA product code for Medical image processing software?

The FDA product code for Medical image processing software is JAK.

Related Clinical Trials

Related PubMed Literature

Related Devices (Code: JAK)

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.