Pro-Tec Containers, Inc.

Pro-Tec Containers, Inc. holds 6 FDA 510(k) medical device clearances, first cleared 1989, most recent 1994.

Top product codes for Pro-Tec Containers, Inc.

FMI — General Hospital5 devices
JKA — Clinical Chemistry1 device

Recent clearances by Pro-Tec Containers, Inc.

K945273 — PRO-TECH DISPOSABLE SHARPS CONTAINERS VNC2Code FMI·1994-12-14
K945274 — PRO-TEC DISPOSABLE SHARPS CONTAINERS IR180 & IR80Code FMI·1994-12-14
K945275 — PRO-TEC DISPOSBLE SHARPS CONTAINERS Q1Code FMI·1994-12-14
K945276 — PRO-TEC DISPOSABLE SHARPS CONTAINERS 5GCode FMI·1994-12-14
K942179 — PRO-TEC DISPOSABLE SHARPS CONTAINERSCode FMI·1994-12-02
K892665 — PRO-JECT(TM) SAFETY NEEDLE HOLDERCode JKA·1989-10-04

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