The following data is part of a premarket notification filed by Neo Metrics, Inc. with the FDA for Vascupuncture Picc Guidewire.
Device ID | K031652 |
510k Number | K031652 |
Device Name: | VASCUPUNCTURE PICC GUIDEWIRE |
Classification | Wire, Guide, Catheter |
Applicant | NEO METRICS, INC. 14800 28TH AVENUE NORTH SUITE 150 Plymouth, MN 55447 |
Contact | Gene Champeau |
Correspondent | Gene Champeau NEO METRICS, INC. 14800 28TH AVENUE NORTH SUITE 150 Plymouth, MN 55447 |
Product Code | DQX |
CFR Regulation Number | 870.1330 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-05-28 |
Decision Date | 2003-09-30 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00816840020234 | K031652 | 000 |
30884908016964 | K031652 | 000 |
30884908145138 | K031652 | 000 |