Nice-Pak Products, Inc.
Nice-Pak Products, Inc. appears in FDA public data with 0 recalls, 9 510(k) clearances, 30 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on January 16, 1998.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 30
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K974768 | PDI STERILE LUBRICATING JELLY | January 16, 1998 |
| K840342 | PDI PREPMASTER WET PACK PATIENT PREP KIT | March 27, 1984 |
| K840343 | PDI PREPMASTER WET PACK VAGINAL-X21477 | March 27, 1984 |
| K840344 | PDI PREPMASTER WET PACK MINOR PROCEDURE | March 26, 1984 |
| K833549 | PDI SURGICAL SCRUB/BRUSH T150-70 | November 28, 1983 |
| K810337 | PDI SURGICAL SCRUB SPONGE-BRUSH-T15070 | February 26, 1981 |
| K781539 | ISO-CARE KIT | November 3, 1978 |
| K780279 | ICE-PAK, PDI | April 10, 1978 |
| K780400 | DEN-Z-ORB | March 27, 1978 |