K821838 is an FDA 510(k) clearance for the VARI-SUPPORT LOW BACK POSTURE PILLOW. This device is classified as a Support, Patient Position (Class I - General Controls, product code CCX).
Submitted by Body Therapeutics, Inc. (Mchenry, US). The FDA issued a Cleared decision on July 20, 1982, 28 days after receiving the submission on June 22, 1982.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.6820.
| 510(k) Number | K821838 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 22, 1982 |
| Decision Date | July 20, 1982 |
| Days to Decision | 28 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | CCX — Support, Patient Position |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 868.6820 |