Shinemound Enterprise, Inc.
Shinemound Enterprise, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2005.
Top product codes for Shinemound Enterprise, Inc.
Recent clearances by Shinemound Enterprise, Inc.
- K051913 — POWDERED LATEX PATIENT EXAMINATION GLOVES
- K994248 — SENSI-PRO, DISPOSABLE PRE-POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES WITH BEIGE PIGMENT ADDITIVES
- K994258 — SENSI-PRO DISPOSABLE POWDER FREE SYNTHETIC VINYL PATIENT EXAMINATION GLOVES WITH BEIGE PIGMENT ADDITIVES
- K993231 — SENSI-PRO DISPOSABLE POWDERED VINYL SYNTHETIC EXAMINATION GLOVES WITH WHITE PIGMENT ADDITIVES
- K993240 — SENSI-PRO DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES WITH WHITE PIGMENT ADDITIVES
- K971360 — SYNTEX
- K972104 — LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES
- K970625 — POLY-MED
Data sourced from openFDA. This site is unofficial and independent of the FDA.