The following data is part of a premarket notification filed by Arrow Intl., Inc. with the FDA for Autocat Intra-aortic Balloon Pump Series.
Device ID | K060309 |
510k Number | K060309 |
Device Name: | AUTOCAT INTRA-AORTIC BALLOON PUMP SERIES |
Classification | System, Balloon, Intra-aortic And Control |
Applicant | ARROW INTL., INC. 9 PLYMOUTH ST. Everett, MA 02149 |
Contact | Karen Provencher |
Correspondent | Karen Provencher ARROW INTL., INC. 9 PLYMOUTH ST. Everett, MA 02149 |
Product Code | DSP |
CFR Regulation Number | 870.3535 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-02-07 |
Decision Date | 2006-04-06 |
Summary: | summary |