Medical Device Manufacturer · US , Puyallup , WA

Tri-Ject Intl. Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2000

Total

Cleared

Denied

Tri-Ject Intl. Corp. has 1 FDA 510(k) cleared medical devices. Based in Puyallup, US.

Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Tri-Ject Intl. Corp. Filter by specialty or product code using the sidebar.

Tri-Ject Intl. Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Tri-Ject Intl. Corp.

1 devices

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