The following data is part of a premarket notification filed by Surgimark, Inc. with the FDA for Via-guard.
Device ID | K871950 |
510k Number | K871950 |
Device Name: | VIA-GUARD |
Classification | Catheter And Tip, Suction |
Applicant | SURGIMARK, INC. 4706 WEST NOB HILL BLVD. Yakima, WA 98908 |
Contact | Richard J Yarger,md |
Correspondent | Richard J Yarger,md SURGIMARK, INC. 4706 WEST NOB HILL BLVD. Yakima, WA 98908 |
Product Code | JOL |
CFR Regulation Number | 880.6740 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-05-20 |
Decision Date | 1987-07-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() VIA-GUARD 73688951 1490047 Live/Registered |
SURGIMARK, INC. 1987-10-13 |