The following data is part of a premarket notification filed by G.d. Searle And Co. with the FDA for Administration Set.
Device ID | K810131 |
510k Number | K810131 |
Device Name: | ADMINISTRATION SET |
Classification | Tube, Feeding |
Applicant | G.D. SEARLE AND CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | FPD |
CFR Regulation Number | 876.5980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-01-19 |
Decision Date | 1981-02-26 |