The following data is part of a premarket notification filed by Future Medical Technologies Intl., Inc. with the FDA for Qualture.
Device ID | K903470 |
510k Number | K903470 |
Device Name: | QUALTURE |
Classification | Kit, Screening, Urine |
Applicant | FUTURE MEDICAL TECHNOLOGIES INTL., INC. 22 VANDEVENTER AVE. Princeton, NJ 08540 |
Contact | Joseph Hippensteel |
Correspondent | Joseph Hippensteel FUTURE MEDICAL TECHNOLOGIES INTL., INC. 22 VANDEVENTER AVE. Princeton, NJ 08540 |
Product Code | JXA |
CFR Regulation Number | 866.2660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-08-01 |
Decision Date | 1990-12-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
QUALTURE 74800409 1897946 Dead/Cancelled |
FUTURE MEDICAL TECHNOLOGIES, INC. 1990-02-09 |
QUALTURE 74027367 1702677 Dead/Cancelled |
Future Medical Technologies, Inc. 1990-02-09 |