Medical Device Manufacturer · US , Mchenry , IL

Nice-Pak Products, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1978

Total

Cleared

Denied

Nice-Pak Products, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1978 to 1998. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Nice-Pak Products, Inc. Filter by specialty or product code using the sidebar.

Nice-Pak Products, Inc. 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 - Nice-Pak Products, Inc.

9 devices

1-9 of 9

Cleared Jan 16, 1998

PDI STERILE LUBRICATING JELLY

K974768 · KMJ

General Hospital · 25d

Cleared Mar 27, 1984

PDI PREPMASTER WET PACK PATIENT PREP KIT

K840342 · FRG

General Hospital · 81d

Cleared Mar 27, 1984

PDI PREPMASTER WET PACK VAGINAL-X21477

K840343 · KGO

General Hospital · 81d

Cleared Mar 26, 1984

PDI PREPMASTER WET PACK MINOR PROCEDURE

K840344 · FRG

General Hospital · 80d

Cleared Nov 28, 1983

PDI SURGICAL SCRUB/BRUSH T150-70

K833549 · NAB

General & Plastic Surgery · 88d

Cleared Feb 26, 1981

PDI SURGICAL SCRUB SPONGE-BRUSH-T15070

K810337 · GEC

General & Plastic Surgery · 17d

Cleared Nov 03, 1978

ISO-CARE KIT

K781539 · HMP

General & Plastic Surgery · 56d

Cleared Apr 10, 1978

ICE-PAK, PDI

K780279 · IMD

Physical Medicine · 48d

Nice-Pak Products, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Nice-Pak Products, Inc.

Filters