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FDA 510(k)

Air Compression Therapy Device, model HW6007

K-Number: K210240 · 2021-02-22

ApplicantKonliking Tech & Dev. Limited
Decision Date2021-02-22
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Air Compression Therapy Device, model HW6007 is a medical device manufactured by Konliking Tech & Dev. Limited. It received FDA 510(k) clearance on 2021-02-22 under approval number K210240. 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 Device, model HW6007?

Air Compression Therapy Device, model HW6007 is a medical device that received FDA 510(k) clearance on 2021-02-22. It is manufactured by Konliking Tech & Dev. Limited. The 510(k) number is K210240.

When was Air Compression Therapy Device, model HW6007 approved by the FDA?

Air Compression Therapy Device, model HW6007 received FDA 510(k) clearance on 2021-02-22, under approval number K210240.

What company makes Air Compression Therapy Device, model HW6007?

Air Compression Therapy Device, model HW6007 is manufactured by Konliking Tech & Dev. Limited.

What is the FDA product code for Air Compression Therapy Device, model HW6007?

The FDA product code for Air Compression Therapy Device, model HW6007 is IRP.

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Related PubMed Literature

PMID: 41915420 Analysis Model for Infant Incubator Adverse Events Using Retrieval-Augmented Generation Combined With Dual-Adapter Fine-Tuning: Development and Evaluation Study. JMIR medical informatics (2026) PMID: 41831468 Cardiometabolic prediction models for young people with psychosis spectrum disorders in the UK (PsyMetRiC 2.0): a retrospective, multicohort clinical prediction model study. The lancet. Psychiatry (2026) PMID: 41501972 First Application of an Eddy-Scale Hemolysis Model to the Food and Drug Administration Nozzle Using Computational Fluid Dynamics. ASAIO journal (American Society for Artificial Internal Organs : 1992) (2026) PMID: 41072144 Use of Bayesian decision analysis in the design of patient-centered clinical trials for kidney failure devices. Computers in biology and medicine (2025)

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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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