The following data is part of a premarket notification filed by American Pharmaseal Div. Ahsc with the FDA for Disposable Transducer Domes & Kits.
Device ID | K821894 |
510k Number | K821894 |
Device Name: | DISPOSABLE TRANSDUCER DOMES & KITS |
Classification | Transducer, Blood-pressure, Extravascular |
Applicant | AMERICAN PHARMASEAL DIV. AHSC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | DRS |
CFR Regulation Number | 870.2850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-06-28 |
Decision Date | 1982-07-20 |