The following data is part of a premarket notification filed by Liquid Crystal Sciences, Inc. with the FDA for Fever Line And Fever Line Plus.
Device ID | K893803 |
510k Number | K893803 |
Device Name: | FEVER LINE AND FEVER LINE PLUS |
Classification | Strip, Temperature, Forehead, Liquid Crystal |
Applicant | LIQUID CRYSTAL SCIENCES, INC. 105/120 INTERSTATE NORTH PARKWAY EAST Atlanta, GA 30339 |
Contact | L Brett |
Correspondent | L Brett LIQUID CRYSTAL SCIENCES, INC. 105/120 INTERSTATE NORTH PARKWAY EAST Atlanta, GA 30339 |
Product Code | KPD |
CFR Regulation Number | 880.2200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-05-22 |
Decision Date | 1989-08-21 |