K200154 is an FDA 510(k) clearance for the B&J DVT Compression Devices MHH800/MHH800SQ. This device is classified as a Sleeve, Limb, Compressible (Class II - Special Controls, product code JOW).
Submitted by B&J Manufacturing , Ltd. (Shenzhen, CN). The FDA issued a Cleared decision on July 8, 2020, 168 days after receiving the submission on January 22, 2020.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.5800.
| 510(k) Number | K200154 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 22, 2020 |
| Decision Date | July 08, 2020 |
| Days to Decision | 168 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | JOW - Sleeve, Limb, Compressible |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.5800 |