Wien Laboratories, Inc.
Wien Laboratories, Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1991.
Top product codes for Wien Laboratories, Inc.
Recent clearances by Wien Laboratories, Inc.
- K912850 — SHBG
- K834246 — PROGESTERONE TEST SET 125I 17-OH
- K832452 — ANDROSTENEDIONE TEST SET 125I
- K823200 — 125 I-DEHYDROEPIANDROSTERONE SULFATE
- K821652 — DOXEPIN TRI-CY TEST SET
- K821653 — PROTRIPTYLINE TRI-CY TEST SET
- K802728 — 125I-TESTOSTERONE TEST SET
- K792041 — DHEA-SULFATE TEST SET
- K781834 — TEST SET, 125 I-DIGOXIN
- K781599 — I-ESTRIOL TEST SET
- K772306 — 125I DIGOXIN TEST SET
- K771793 — DHEA TEST SET
- K771729 — 17-HYDROXYPROGESTERONE TEST SET
Data sourced from openFDA. This site is unofficial and independent of the FDA.