The following data is part of a premarket notification filed by Boston Scientific Corp. with the FDA for Renegade Fiber Braided Microcatheter.
Device ID | K973645 |
510k Number | K973645 |
Device Name: | RENEGADE FIBER BRAIDED MICROCATHETER |
Classification | Catheter, Continuous Flush |
Applicant | BOSTON SCIENTIFIC CORP. ONE BOSTON SCIENTIFIC PL. Natick, MA 01760 -1537 |
Contact | Wanda M Carpinella |
Correspondent | Wanda M Carpinella BOSTON SCIENTIFIC CORP. ONE BOSTON SCIENTIFIC PL. Natick, MA 01760 -1537 |
Product Code | KRA |
CFR Regulation Number | 870.1210 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-09-24 |
Decision Date | 1997-11-19 |
Summary: | summary |