The following data is part of a premarket notification filed by Kendall Research Center with the FDA for T.e.d. Sequential Compression Sleeves.
| Device ID | K781357 |
| 510k Number | K781357 |
| Device Name: | T.E.D. SEQUENTIAL COMPRESSION SLEEVES |
| Classification | Sleeve, Limb, Compressible |
| Applicant | KENDALL RESEARCH CENTER 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JOW |
| CFR Regulation Number | 870.5800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-08-08 |
| Decision Date | 1978-09-20 |