K012614 is an FDA 510(k) clearance for the KENDALL, SEQUENTIAL COMPRESSION DEVICE. This device is classified as a Sleeve, Limb, Compressible (Class II - Special Controls, product code JOW).
Submitted by Medical Instruments Technology, Inc. (St. George, US). The FDA issued a Cleared decision on May 1, 2002, 261 days after receiving the submission on August 13, 2001.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.5800.
| 510(k) Number | K012614 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 13, 2001 |
| Decision Date | May 01, 2002 |
| Days to Decision | 261 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 |