Veinoflow SCD (Model: LBTK-M-I 5006)
K-Number: K213313 · 2022-02-09
Decision Date2022-02-09
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Veinoflow SCD (Model: LBTK-M-I 5006) is a medical device manufactured by Dalian Labtek Science & Development Co., Ltd.. It received FDA 510(k) clearance on 2022-02-09 under approval number K213313. 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 Veinoflow SCD (Model: LBTK-M-I 5006)?
Veinoflow SCD (Model: LBTK-M-I 5006) is a medical device that received FDA 510(k) clearance on 2022-02-09. It is manufactured by Dalian Labtek Science & Development Co., Ltd.. The 510(k) number is K213313.
When was Veinoflow SCD (Model: LBTK-M-I 5006) approved by the FDA?
Veinoflow SCD (Model: LBTK-M-I 5006) received FDA 510(k) clearance on 2022-02-09, under approval number K213313.
What company makes Veinoflow SCD (Model: LBTK-M-I 5006)?
Veinoflow SCD (Model: LBTK-M-I 5006) is manufactured by Dalian Labtek Science & Development Co., Ltd..
What is the FDA product code for Veinoflow SCD (Model: LBTK-M-I 5006)?
The FDA product code for Veinoflow SCD (Model: LBTK-M-I 5006) 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.