The following data is part of a premarket notification filed by Cottrell, Ltd. with the FDA for Procide 14 N.s., Omnicide/liquid & Plus Liq Activator.
| Device ID | K932922 |
| 510k Number | K932922 |
| Device Name: | PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR |
| Classification | Sterilant, Medical Devices |
| Applicant | COTTRELL, LTD. 7399 SOUTH TUCSON WAY Englewood, CO 80112 |
| Contact | Jack Scoville |
| Correspondent | Jack Scoville COTTRELL, LTD. 7399 SOUTH TUCSON WAY Englewood, CO 80112 |
| Product Code | MED |
| CFR Regulation Number | 880.6885 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-15 |
| Decision Date | 1995-07-03 |