The following data is part of a premarket notification filed by Paco Research Corp. with the FDA for A Family Of Tracheobronchial Suction Catheter Prod.
Device ID | K850032 |
510k Number | K850032 |
Device Name: | A FAMILY OF TRACHEOBRONCHIAL SUCTION CATHETER PROD |
Classification | Catheters, Suction, Tracheobronchial |
Applicant | PACO RESEARCH CORP. ELLIS PHARMACEUTICAL CONSULTIN 913 STATE ROAD Princeton, NJ 08540 |
Contact | Levi Ellis |
Correspondent | Levi Ellis PACO RESEARCH CORP. ELLIS PHARMACEUTICAL CONSULTIN 913 STATE ROAD Princeton, NJ 08540 |
Product Code | BSY |
CFR Regulation Number | 868.6810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-01-07 |
Decision Date | 1985-02-01 |