The following data is part of a premarket notification filed by Venetec, Inc. with the FDA for Statlock Iv Connector And Anchor Set.
Device ID | K902109 |
510k Number | K902109 |
Device Name: | STATLOCK IV CONNECTOR AND ANCHOR SET |
Classification | Set, Administration, Intravascular |
Applicant | VENETEC, INC. 1250 SOUTH PARKER RD. SUITE 204, P.O. BOX 6510 Denver, CO 80206 |
Contact | David C Howson |
Correspondent | David C Howson VENETEC, INC. 1250 SOUTH PARKER RD. SUITE 204, P.O. BOX 6510 Denver, CO 80206 |
Product Code | FPA |
CFR Regulation Number | 880.5440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-05-09 |
Decision Date | 1990-10-19 |