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)

LF900

K-Number: K203019 · 2021-06-22

ApplicantDaesung Maref Co., Ltd.
Decision Date2021-06-22
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LF900 is a medical device manufactured by Daesung Maref Co., Ltd.. It received FDA 510(k) clearance on 2021-06-22 under approval number K203019. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LF900?

LF900 is a medical device that received FDA 510(k) clearance on 2021-06-22. It is manufactured by Daesung Maref Co., Ltd.. The 510(k) number is K203019.

When was LF900 approved by the FDA?

LF900 received FDA 510(k) clearance on 2021-06-22, under approval number K203019.

What company makes LF900?

LF900 is manufactured by Daesung Maref Co., Ltd..

What is the FDA product code for LF900?

The FDA product code for LF900 is IRP.

Other Devices by Daesung Maref Co., Ltd.

K160180Intermittent Pneumatic Compression system K150980Venous Assist System K160178Lympha-Flow(LF1200) K203016DVT-2600 K202395SP-1000, SP-2000 K203498LX9max

View all 10 devices →

Related Devices (Code: IRP)

K160608NormaTec Pulse and NormaTec Pulse ProNormaTec Industries, LP K171685Med4 EliteCool Systems, Inc. (Dba Game Ready) K161907Pressure Therapy SystemXiamen Senyang Co., Ltd. K163280RP Lite 760RMego Afek AC , Ltd. K160178Lympha-Flow(LF1200)Daesung Maref Co., Ltd. K183169Pulse 2.0, Pulse Pro 2.0NormaTec Industries, LP

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.

↑