The following data is part of a premarket notification filed by Julius Zorn, Inc. with the FDA for Juzo-respira Anti-embolism Stocking.
| Device ID | K905413 |
| 510k Number | K905413 |
| Device Name: | JUZO-RESPIRA ANTI-EMBOLISM STOCKING |
| Classification | Stocking, Medical Support (to Prevent Pooling Of Blood In Legs) |
| Applicant | JULIUS ZORN, INC. 355 SOUTH GRAND AVE. SUITE 3000 Los Angeles, CA 90071 |
| Contact | Vicki L Cresap |
| Correspondent | Vicki L Cresap JULIUS ZORN, INC. 355 SOUTH GRAND AVE. SUITE 3000 Los Angeles, CA 90071 |
| Product Code | DWL |
| CFR Regulation Number | 880.5780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-12-03 |
| Decision Date | 1991-05-17 |