The following data is part of a premarket notification filed by Sil-med Corp. with the FDA for Vascular Access Catheter.
Device ID | K851195 |
510k Number | K851195 |
Device Name: | VASCULAR ACCESS CATHETER |
Classification | Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days |
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 | LJS |
CFR Regulation Number | 880.5970 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-03-26 |
Decision Date | 1985-06-07 |