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)

Venowave VW5

K-Number: K232640 · 2024-06-25

ApplicantThermabright
Decision Date2024-06-25
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Venowave VW5 is a medical device manufactured by Thermabright. It received FDA 510(k) clearance on 2024-06-25 under approval number K232640. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Venowave VW5?

Venowave VW5 is a medical device that received FDA 510(k) clearance on 2024-06-25. It is manufactured by Thermabright. The 510(k) number is K232640.

When was Venowave VW5 approved by the FDA?

Venowave VW5 received FDA 510(k) clearance on 2024-06-25, under approval number K232640.

What company makes Venowave VW5?

Venowave VW5 is manufactured by Thermabright.

What is the FDA product code for Venowave VW5?

The FDA product code for Venowave VW5 is JOW.

Related Devices (Code: JOW)

K163055Reprocessed Kendall SCD Express Foot CuffCovidien K160180Intermittent Pneumatic Compression systemDaesung Maref Co., Ltd. K161105Reprocessed Compression GarmentsCovidien K160431ActiveCare HomeMedical Compression Systems (Dbn) , Ltd. K161346NormaTec PCD-T and PCD-BNormaTec Industries, LP K161209Cirona 6400Devon Medical Products

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.

↑