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 |