The following data is part of a premarket notification filed by Sheridan Catheter Corp. with the FDA for Tracheobronchial Suction Catheter.
Device ID | K860802 |
510k Number | K860802 |
Device Name: | TRACHEOBRONCHIAL SUCTION CATHETER |
Classification | Catheters, Suction, Tracheobronchial |
Applicant | SHERIDAN CATHETER CORP. ROUTE 40 Argyle, NY 12809 |
Contact | Steen, Ph.d. |
Correspondent | Steen, Ph.d. SHERIDAN CATHETER CORP. ROUTE 40 Argyle, NY 12809 |
Product Code | BSY |
CFR Regulation Number | 868.6810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-03-04 |
Decision Date | 1986-04-02 |