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 |