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)

Hisense LCD monitor HMD2C21A, HMD4C27S, HMD6C30D

K-Number: K222208 · 2022-11-17

Decision Date2022-11-17
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Hisense LCD monitor HMD2C21A, HMD4C27S, HMD6C30D is the device name listed in this FDA 510(k) record. The listed applicant is Qingdao Hisense Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2022-11-17 under 510(k) number K222208. The device is classified under product code PGY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Hisense LCD monitor HMD2C21A, HMD4C27S, HMD6C30D?

Hisense LCD monitor HMD2C21A, HMD4C27S, HMD6C30D is a medical device that received FDA 510(k) clearance on 2022-11-17. The listed applicant is Qingdao Hisense Medical Equipment Co., Ltd.. The 510(k) number is K222208.

When did Hisense LCD monitor HMD2C21A, HMD4C27S, HMD6C30D receive FDA 510(k) clearance?

Hisense LCD monitor HMD2C21A, HMD4C27S, HMD6C30D received FDA 510(k) clearance on 2022-11-17, under 510(k) number K222208.

Who is the listed applicant for Hisense LCD monitor HMD2C21A, HMD4C27S, HMD6C30D?

The FDA 510(k) record lists Qingdao Hisense Medical Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Hisense LCD monitor HMD2C21A, HMD4C27S, HMD6C30D?

The FDA product code for Hisense LCD monitor HMD2C21A, HMD4C27S, HMD6C30D is PGY.

Other records listing Qingdao Hisense Medical Equipment Co., Ltd. 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.

View all 7 devices →

Related Devices (Code: PGY)

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.

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.