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FDA 510(k)

Air compression therapy system FO3002

K-Number: K212169 · 2021-11-23

ApplicantFoshan Hongfeng Co., Ltd.
Decision Date2021-11-23
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Air compression therapy system FO3002 is a medical device manufactured by Foshan Hongfeng Co., Ltd.. It received FDA 510(k) clearance on 2021-11-23 under approval number K212169. 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 Air compression therapy system FO3002?

Air compression therapy system FO3002 is a medical device that received FDA 510(k) clearance on 2021-11-23. It is manufactured by Foshan Hongfeng Co., Ltd.. The 510(k) number is K212169.

When was Air compression therapy system FO3002 approved by the FDA?

Air compression therapy system FO3002 received FDA 510(k) clearance on 2021-11-23, under approval number K212169.

What company makes Air compression therapy system FO3002?

Air compression therapy system FO3002 is manufactured by Foshan Hongfeng Co., Ltd..

What is the FDA product code for Air compression therapy system FO3002?

The FDA product code for Air compression therapy system FO3002 is IRP.

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Related PubMed Literature

PMID: 41966529 Comparison of the AccuPower HIV-1 Quant Kit and Aptima HIV-1 Quant Dx Assay for quantification of HIV-1 plasma viral load. Diagnostic microbiology and infectious disease (2026) PMID: 40942702 Digital Cardiovascular Twins, AI Agents, and Sensor Data: A Narrative Review from System Architecture to Proactive Heart Health. Sensors (Basel, Switzerland) (2025) PMID: 40624966 Peptide-Enhanced Bioactive Hydrogel Combined with Photodynamic-Phage Synergistic Antibacterial Therapy System Accelerates Infected Wound Healing. Advanced healthcare materials (2025)

Other Devices by Foshan Hongfeng Co., Ltd.

K201982Air compression therapy system FO-3001; Air compression therapy system FO-3008

Related Devices (Code: IRP)

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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.

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