The following data is part of a premarket notification filed by Datascope Corp. with the FDA for Datascope Percor Stat-mil 9.5 Fr Intra-aortic Ball.
Device ID | K880289 |
510k Number | K880289 |
Device Name: | DATASCOPE PERCOR STAT-MIL 9.5 FR INTRA-AORTIC BALL |
Classification | System, Balloon, Intra-aortic And Control |
Applicant | DATASCOPE CORP. 3 FIR CT. P.O. BOX 3100 Oakland, NJ 07436 |
Contact | Schneider, Phd |
Correspondent | Schneider, Phd DATASCOPE CORP. 3 FIR CT. P.O. BOX 3100 Oakland, NJ 07436 |
Product Code | DSP |
CFR Regulation Number | 870.3535 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-01-25 |
Decision Date | 1988-06-10 |