B&J DVT Compression Devices MHH800/MHH800SQ
K-Number: K200154 · 2020-07-08
Device Summary
Frequently Asked Questions
What is the B&J DVT Compression Devices MHH800/MHH800SQ?
B&J DVT Compression Devices MHH800/MHH800SQ is a medical device that received FDA 510(k) clearance on 2020-07-08. The listed applicant is B&J Manufacturing , Ltd.. The 510(k) number is K200154.
When did B&J DVT Compression Devices MHH800/MHH800SQ receive FDA 510(k) clearance?
B&J DVT Compression Devices MHH800/MHH800SQ received FDA 510(k) clearance on 2020-07-08, under 510(k) number K200154.
Who is the listed applicant for B&J DVT Compression Devices MHH800/MHH800SQ?
The FDA 510(k) record lists B&J Manufacturing , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for B&J DVT Compression Devices MHH800/MHH800SQ?
The FDA product code for B&J DVT Compression Devices MHH800/MHH800SQ is JOW.
Other records listing B&J Manufacturing , Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JOW)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.