The following data is part of a premarket notification filed by Laser Peripherals Llc. with the FDA for Laseguide 600a, 600b, 400a, 400b For Pulmonary Use.
| Device ID | K880592 |
| 510k Number | K880592 |
| Device Name: | LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE |
| Classification | Laser, Neodymium:yag, Pulmonary Surgery |
| Applicant | LASER PERIPHERALS LLC. 35 POND PARK RD. #9 Hingham, MA 02043 |
| Contact | Michael N Basel |
| Correspondent | Michael N Basel LASER PERIPHERALS LLC. 35 POND PARK RD. #9 Hingham, MA 02043 |
| Product Code | LLO |
| CFR Regulation Number | 874.4500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-02-11 |
| Decision Date | 1988-04-25 |