The following data is part of a premarket notification filed by Medical Products Development, Inc. with the FDA for Surg-flex 10 Light.
| Device ID | K803067 |
| 510k Number | K803067 |
| Device Name: | SURG-FLEX 10 LIGHT |
| Classification | Light, Surgical, Instrument |
| Applicant | MEDICAL PRODUCTS DEVELOPMENT, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FSQ |
| CFR Regulation Number | 878.4580 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-12-04 |
| Decision Date | 1981-02-26 |