The following data is part of a premarket notification filed by Medcomp (dba Medical Components, Inc.) with the FDA for 20g X 5/8 Pro-lock Ct Safety Infusion Set.
Device ID | K171333 |
510k Number | K171333 |
Device Name: | 20G X 5/8 Pro-Lock CT Safety Infusion Set |
Classification | Non-coring (huber) Needle |
Applicant | Medcomp (dba Medical Components, Inc.) 1499 Delp Drive Harleysville, PA 19438 |
Contact | Courtney Nix |
Correspondent | Courtney Nix Medcomp (dba Medical Components, Inc.) 1499 Delp Drive Harleysville, PA 19438 |
Product Code | PTI |
CFR Regulation Number | 880.5570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-05-08 |
Decision Date | 2017-07-18 |
Summary: | summary |