Lubricating Jelly
by H & P Industries, Inc. 510(k)
Active
510(k) K871169
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK871169 | Date1 Apr 1987 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
-
- Terminated Z-2013-2011
Possible contamination due to sterilization issue. Inspection of contract manufacturer found cGMP deficiencies.
-
- Terminated Z-0934-2011
Triad Group is recalling all lots of Sterile Lubricating Jelly manufactured by Triad Group. This recall has been initiated due to concerns expressed by the Food and Drug Administration regarding the validation of the gamma radiation sterilization cycles for these products.
Specification
- 510(k) Number
- FDA Product Code
- KMJ
- Device Class
- Class I
- Regulation
- 21 CFR Part 880.6375
- Advisory Committee
- General Hospital
- FDA Decision
- SESE Substantially Equivalent