The following data is part of a premarket notification filed by Phx Technologies Corp. with the FDA for Trocar.
Device ID | K940687 |
510k Number | K940687 |
Device Name: | TROCAR |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | PHX TECHNOLOGIES CORP. POST OFFICE BOX 1059 Lewisville, TX 75067 |
Contact | James F Chapel |
Correspondent | James F Chapel PHX TECHNOLOGIES CORP. POST OFFICE BOX 1059 Lewisville, TX 75067 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-02-16 |
Decision Date | 1994-03-16 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TROCAR 86526529 4812059 Live/Registered |
FERADYNE OUTDOORS, LLC 2015-02-06 |