The following data is part of a premarket notification filed by Morrison Medical Products with the FDA for Morrison Medical Wrist Restraint.
| Device ID | K963419 |
| 510k Number | K963419 |
| Device Name: | MORRISON MEDICAL WRIST RESTRAINT |
| Classification | Restraint, Protective |
| Applicant | MORRISON MEDICAL PRODUCTS 2000 HOLLISTER DR. Libertyville, IL 60048 |
| Contact | Joseph S Tokarz |
| Correspondent | Joseph S Tokarz MORRISON MEDICAL PRODUCTS 2000 HOLLISTER DR. Libertyville, IL 60048 |
| Product Code | FMQ |
| CFR Regulation Number | 880.6760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-08-30 |
| Decision Date | 1996-10-31 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00647921011724 | K963419 | 000 |