The following data is part of a premarket notification filed by Kendall Research Center with the FDA for Tray, Curity Continuous Epidural.
Device ID | K760343 |
510k Number | K760343 |
Device Name: | TRAY, CURITY CONTINUOUS EPIDURAL |
Classification | Anesthesia Conduction Kit |
Applicant | KENDALL RESEARCH CENTER 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | CAZ |
CFR Regulation Number | 868.5140 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1976-07-30 |
Decision Date | 1976-08-11 |