The following data is part of a premarket notification filed by Medical Instrument Development Laboratories, Inc. with the FDA for Infusion Cannula.
| Device ID | K831192 |
| 510k Number | K831192 |
| Device Name: | INFUSION CANNULA |
| Classification | Cannula, Ophthalmic |
| Applicant | MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HMX |
| CFR Regulation Number | 886.4350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-04-12 |
| Decision Date | 1983-06-30 |