The following data is part of a premarket notification filed by Akcess Medical Products, Inc. with the FDA for Y Adaptor.
Device ID | K910321 |
510k Number | K910321 |
Device Name: | Y ADAPTOR |
Classification | Accessories, Blood Circuit, Hemodialysis |
Applicant | AKCESS MEDICAL PRODUCTS, INC. 789 JERSEY AVE. New Brunswick, NJ 08901 |
Contact | Balbir B Kapany |
Correspondent | Balbir B Kapany AKCESS MEDICAL PRODUCTS, INC. 789 JERSEY AVE. New Brunswick, NJ 08901 |
Product Code | KOC |
CFR Regulation Number | 876.5820 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-01-24 |
Decision Date | 1991-04-16 |