Medical Device Manufacturer · CA , Canada H3a 2n4

Pharma-Plast USA, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1985

Total

Cleared

Denied

Pharma-Plast USA, Inc. has 9 FDA 510(k) cleared medical devices. Based in Canada H3a 2n4, CA.

Historical record: 9 cleared submissions from 1985 to 1989. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Pharma-Plast USA, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pharma-Plast USA, Inc.

9 devices

1-9 of 9

Cleared Oct 25, 1989

NIPRO SAFELET CATH

K894371 · FOZ

General Hospital · 100d

PHARMA-PLAST INSULIN INFUSION SET

K884978 · LZG

General Hospital · 203d

Cleared Jun 15, 1987

MULTIPLE PHARMA-PLAST TRACHEAL TUBE

K871263 · BTR

Anesthesiology · 76d

Cleared Oct 16, 1985

PHARMA-PLAST CLINIPAK

K852443 · FMF

General Hospital · 128d

Cleared Oct 16, 1985

ASIK 'ONCE' SYRINGE

K852444 · FMF

General Hospital · 128d

Cleared Sep 20, 1985

PHARMA-PLAST NEEDLE

K852442 · FMI

General Hospital · 102d

Pharma-Plast USA, Inc. - FDA 510(k) Cleared Devices

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