DIALATORS PC-203 & 202

System, Peritoneal, Automatic Delivery

MEDIGROUP

The following data is part of a premarket notification filed by Medigroup with the FDA for Dialators Pc-203 & 202.

Pre-market Notification Details

Device IDK823330
510k NumberK823330
Device Name:DIALATORS PC-203 & 202
ClassificationSystem, Peritoneal, Automatic Delivery
Applicant MEDIGROUP 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeFKX  
CFR Regulation Number876.5630 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-11-08
Decision Date1983-01-26

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