Company ยท US
Nice-Pak Products, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1998. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jan 16, 1998 | K974768 | PDI STERILE LUBRICATING JELLY Nice-Pak Products, Inc. | KMJ |
| Mar 27, 1984 | K840343 | PDI PREPMASTER WET PACK VAGINAL-X21477 Nice-Pak Products, Inc. | KGO |
| Mar 27, 1984 | K840342 | PDI PREPMASTER WET PACK PATIENT PREP KIT Nice-Pak Products, Inc. | FRG |
| Mar 26, 1984 | K840344 | PDI PREPMASTER WET PACK MINOR PROCEDURE Nice-Pak Products, Inc. | FRG |
| Nov 28, 1983 | K833549 | PDI SURGICAL SCRUB/BRUSH T150-70 Nice-Pak Products, Inc. | NAB |
| Feb 26, 1981 | K810337 | PDI SURGICAL SCRUB SPONGE-BRUSH-T15070 Nice-Pak Products, Inc. | GEC |
| Nov 3, 1978 | K781539 | ISO-CARE KIT Nice-Pak Products, Inc. | HMP |
| Apr 10, 1978 | K780279 | ICE-PAK, PDI Nice-Pak Products, Inc. | IMD |
| Mar 27, 1978 | K780400 | DEN-Z-ORB Nice-Pak Products, Inc. | KHR |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||