The following data is part of a premarket notification filed by Uresil Corp. with the FDA for Uresil Locking General Purpose Drainage Catheter.
Device ID | K920510 |
510k Number | K920510 |
Device Name: | URESIL LOCKING GENERAL PURPOSE DRAINAGE CATHETER |
Classification | Suture, Nonabsorbable, Synthetic, Polyamide |
Applicant | URESIL CORP. 5418 W. TOUHY AVE. Skokie, IL 60077 |
Contact | Lev Melinyshyn |
Correspondent | Lev Melinyshyn URESIL CORP. 5418 W. TOUHY AVE. Skokie, IL 60077 |
Product Code | GAR |
CFR Regulation Number | 878.5020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-02-02 |
Decision Date | 1992-09-14 |