The following data is part of a premarket notification filed by Dhd Diemolding Healthcare Div. with the FDA for Therapep.
Device ID | K944900 |
510k Number | K944900 |
Device Name: | THERAPEP |
Classification | Spirometer, Therapeutic (incentive) |
Applicant | DHD DIEMOLDING HEALTHCARE DIV. 125 RASBACH ST. Canastota, NY 13032 |
Contact | Jean Wallace |
Correspondent | Jean Wallace DHD DIEMOLDING HEALTHCARE DIV. 125 RASBACH ST. Canastota, NY 13032 |
Product Code | BWF |
CFR Regulation Number | 868.5690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-10-04 |
Decision Date | 1995-01-06 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
THERAPEP 74507290 1993875 Live/Registered |
SMITHS MEDICAL ASD, INC. 1994-03-31 |