Shinemound Enterprise, Inc.
FDA 510(k) medical device clearances.
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.