The following data is part of a premarket notification filed by Sil-med Corp. with the FDA for Incision Drain.
Device ID | K851196 |
510k Number | K851196 |
Device Name: | INCISION DRAIN |
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 | 1985-03-26 |
Decision Date | 1985-06-04 |