The following data is part of a premarket notification filed by Ohmeda Medical with the FDA for Ohmeda Medical Spot Pt Lite Phototherapy System.
Device ID | K011549 |
510k Number | K011549 |
Device Name: | OHMEDA MEDICAL SPOT PT LITE PHOTOTHERAPY SYSTEM |
Classification | Unit, Neonatal Phototherapy |
Applicant | OHMEDA MEDICAL 8880 GORMAN RD. Laurel, MD 20723 |
Contact | Alberto F Profumo |
Correspondent | Alberto F Profumo OHMEDA MEDICAL 8880 GORMAN RD. Laurel, MD 20723 |
Product Code | LBI |
CFR Regulation Number | 880.5700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-05-18 |
Decision Date | 2001-07-19 |