Bioteque America, Inc.
Bioteque America, Inc. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 2004.
Top product codes for Bioteque America, Inc.
Recent clearances by Bioteque America, Inc.
- K041094 — HSG CATHETER SET
- K020628 — CURELLE, PREFERRED CURELLE, CUTEQ 2.5
- K013289 — BIOTEQUE VAGINAL PESSARIES
- K003380 — BIOTEQUE VAGINAL DILATOR
- K920633 — PESSARY FLEXIBLE SILICONE NICHOLS
- K920747 — PESSARY FLEXIBLE SILICONE DONUT RING
- K933628 — CYTOLOGY BRUSH
- K933521 — SPECULUM
- K920187 — FLEXIBLE SILICONE GELIHORN
- K920177 — VERSA-VIAL
Data sourced from openFDA. This site is unofficial and independent of the FDA.