HANDTYMP
Tester, Auditory Impedance
LIFE-TECH INTL., INC.
The following data is part of a premarket notification filed by Life-tech Intl., Inc. with the FDA for Handtymp.
Pre-market Notification Details
| Device ID | K923072 |
| 510k Number | K923072 |
| Device Name: | HANDTYMP |
| Classification | Tester, Auditory Impedance |
| Applicant | LIFE-TECH INTL., INC. P.O. BOX 36221 Houston, TX 77236 -6221 |
| Contact | Alfred C Coats |
| Correspondent | Alfred C Coats LIFE-TECH INTL., INC. P.O. BOX 36221 Houston, TX 77236 -6221 |
| Product Code | ETY |
| CFR Regulation Number | 874.1090 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-06-25 |
| Decision Date | 1993-03-18 |
Trademark Results [HANDTYMP]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 HANDTYMP 73795572 1623489 Dead/Cancelled |
REXTON DANPLEX AKTIESELSKAB 1989-04-24 |
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