The following data is part of a premarket notification filed by Sil-med Corp. with the FDA for Y Connector.
Device ID | K851921 |
510k Number | K851921 |
Device Name: | Y CONNECTOR |
Classification | Connector, Catheter |
Applicant | SIL-MED CORP. 700 WARNER BLVD. Taunton, MA 02780 |
Contact | Robert Brennan |
Correspondent | Robert Brennan SIL-MED CORP. 700 WARNER BLVD. Taunton, MA 02780 |
Product Code | GCD |
CFR Regulation Number | 878.4200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-05-02 |
Decision Date | 1985-05-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
Y CONNECTOR 73095840 1124868 Dead/Cancelled |
BRAD HARRISON COMPANY 1976-08-06 |