The following data is part of a premarket notification filed by Innomed Corp. with the FDA for Laser Centering Device.
| Device ID | K872747 |
| 510k Number | K872747 |
| Device Name: | LASER CENTERING DEVICE |
| Classification | Marker, Ocular |
| Applicant | INNOMED CORP. 620 LUNAR Brea, CA 92621 |
| Contact | Peter K Brown |
| Correspondent | Peter K Brown INNOMED CORP. 620 LUNAR Brea, CA 92621 |
| Product Code | HMR |
| CFR Regulation Number | 886.4570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-07-13 |
| Decision Date | 1987-09-04 |