Care-Pro Industries, Inc.

Care-Pro Industries, Inc. holds 2 FDA 510(k) medical device clearances, cleared in 1989.

Top product codes for Care-Pro Industries, Inc.

KGO — General, Plastic Surgery1 device
LYY — General Hospital1 device

Recent clearances by Care-Pro Industries, Inc.

K892495 — SURGEON'S GLOVESCode KGO·1989-10-11
K892772 — NON-STERILE PATIENT EXAMINATION GLOVESCode LYY·1989-08-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.