The following data is part of a premarket notification filed by Knight Medical, Inc. with the FDA for Enteral Feeding Sets For Gravity And Pump Use.
Device ID | K862489 |
510k Number | K862489 |
Device Name: | ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE |
Classification | Tubes, Gastrointestinal (and Accessories) |
Applicant | KNIGHT MEDICAL, INC. 335 NEWBURY ST. Boston, MA 02115 |
Contact | Stephen Sutton |
Correspondent | Stephen Sutton KNIGHT MEDICAL, INC. 335 NEWBURY ST. Boston, MA 02115 |
Product Code | KNT |
CFR Regulation Number | 876.5980 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-06-30 |
Decision Date | 1986-09-23 |