The following data is part of a premarket notification filed by Volu Sol Medical Industries with the FDA for Volu-sol Orange G-6(gills-mod.
| Device ID | K822038 |
| 510k Number | K822038 |
| Device Name: | VOLU-SOL ORANGE G-6(GILLS-MOD |
| Classification | Orange G |
| Applicant | VOLU SOL MEDICAL INDUSTRIES 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HZH |
| CFR Regulation Number | 864.1850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-07-12 |
| Decision Date | 1982-08-03 |