The following data is part of a premarket notification filed by Burton Medical Products Corp. with the FDA for Light, Head, Examination.
Device ID | K901706 |
510k Number | K901706 |
Device Name: | LIGHT, HEAD, EXAMINATION |
Classification | Device, Medical Examination, Ac Powered |
Applicant | BURTON MEDICAL PRODUCTS CORP. 7922 HASKELL AVE. Van Nuys, CA 91406 |
Contact | Lani Tonnu |
Correspondent | Lani Tonnu BURTON MEDICAL PRODUCTS CORP. 7922 HASKELL AVE. Van Nuys, CA 91406 |
Product Code | KZF |
CFR Regulation Number | 880.6320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-04-12 |
Decision Date | 1990-07-19 |