The following data is part of a premarket notification filed by Sunsor, Inc. with the FDA for Sunsor Ultraviolet Meter.
Device ID | K934728 |
510k Number | K934728 |
Device Name: | SUNSOR ULTRAVIOLET METER |
Classification | Detector, Ultraviolet |
Applicant | SUNSOR, INC. 1388 FREEPORT RD. Pittsburgh, PA 15238 |
Contact | Stephen J Sherwin |
Correspondent | Stephen J Sherwin SUNSOR, INC. 1388 FREEPORT RD. Pittsburgh, PA 15238 |
Product Code | EAQ |
CFR Regulation Number | 872.6350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-09-29 |
Decision Date | 1994-07-28 |