The following data is part of a premarket notification filed by American Pharmaseal Div. Ahsc with the FDA for Am. Ph. Sterile Feeding Tube.
Device ID | K820420 |
510k Number | K820420 |
Device Name: | AM. PH. STERILE FEEDING TUBE |
Classification | Tubes, Gastrointestinal (and Accessories) |
Applicant | AMERICAN PHARMASEAL DIV. AHSC 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | KNT |
CFR Regulation Number | 876.5980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-02-16 |
Decision Date | 1982-03-23 |