The following data is part of a premarket notification filed by Chattanooga Group, Inc. with the FDA for Intermittent Compression Pumps.
| Device ID | K832920 |
| 510k Number | K832920 |
| Device Name: | INTERMITTENT COMPRESSION PUMPS |
| Classification | Massager, Powered Inflatable Tube |
| Applicant | CHATTANOOGA GROUP, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | IRP |
| CFR Regulation Number | 890.5650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-08-22 |
| Decision Date | 1983-11-07 |