The following data is part of a premarket notification filed by Travenol Laboratories, S.a. with the FDA for Capd Ultraviolet Germicidal Exchange.
Device ID | K833595 |
510k Number | K833595 |
Device Name: | CAPD ULTRAVIOLET GERMICIDAL EXCHANGE |
Classification | System, Peritoneal, Automatic Delivery |
Applicant | TRAVENOL LABORATORIES, S.A. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | FKX |
CFR Regulation Number | 876.5630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-10-12 |
Decision Date | 1983-11-29 |