The following data is part of a premarket notification filed by Covidien Llc with the FDA for Kendall Scd 700 Sequential Compression Controller.
| Device ID | K102737 |
| 510k Number | K102737 |
| Device Name: | KENDALL SCD 700 SEQUENTIAL COMPRESSION CONTROLLER |
| Classification | Sleeve, Limb, Compressible |
| Applicant | Covidien LLC 15 HAMPSHIRE ST Mansfield, MA 02048 |
| Contact | Melody Bi |
| Correspondent | Melody Bi Covidien LLC 15 HAMPSHIRE ST Mansfield, MA 02048 |
| Product Code | JOW |
| CFR Regulation Number | 870.5800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-09-22 |
| Decision Date | 2010-10-19 |
| Summary: | summary |