The following data is part of a premarket notification filed by Zimmar Consulting Ltd. with the FDA for Pharma-plast Urinary Drainage Bag 2000.
Device ID | K843480 |
510k Number | K843480 |
Device Name: | PHARMA-PLAST URINARY DRAINAGE BAG 2000 |
Classification | Collector, Urine, (and Accessories) For Indwelling Catheter |
Applicant | ZIMMAR CONSULTING LTD. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | KNX |
CFR Regulation Number | 876.5250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-09-06 |
Decision Date | 1984-10-11 |