Medical Device Manufacturer · US , Mchenry , IL

Stan-Pak Ent. - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 1982

Total

Cleared

Denied

Stan-Pak Ent. has 20 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 20 cleared submissions from 1982 to 1982. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Stan-Pak Ent. Filter by specialty or product code using the sidebar.

Stan-Pak Ent. 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 - Stan-Pak Ent.

20 devices

1-12 of 20

Cleared Dec 09, 1982

DOSOMETRIC RELEASE STERILIZATION

K823058 · EFQ

General & Plastic Surgery · 52d

General & Plastic Surgery · 28d

Cleared Feb 12, 1982

GUAZE SPONGES, PLAIN

K820107 · EFQ

General & Plastic Surgery · 28d

Cleared Feb 12, 1982

TOPPER SPONGES

K820108 · NAB

General & Plastic Surgery · 28d

Cleared Feb 12, 1982

WEBRIL CAST PADDING

K820140 · ITG

Physical Medicine · 24d

Cleared Feb 12, 1982

SPECIALIST CAST PADDING

K820155 · ITG

Physical Medicine · 24d

Cleared Feb 05, 1982

TELFA STRIPS

K820056 · NAB

General & Plastic Surgery · 25d

Cleared Feb 05, 1982

COMBINE PAD OR ABD

K820105 · NAB

General & Plastic Surgery · 21d

Cleared Feb 05, 1982

SOF-ROL CAST PADDING

K820139 · NAB

General & Plastic Surgery · 17d

Cleared Feb 05, 1982

BIAS STOCKINETTE

K820141 · FQM

General Hospital · 17d

Stan-Pak Ent. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Stan-Pak Ent.

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