The following data is part of a premarket notification filed by Datascope Corp. with the FDA for Percor Stat-dl 9.5 Fr W/opt Insert W/o Intro Sheat.
Device ID | K905056 |
510k Number | K905056 |
Device Name: | PERCOR STAT-DL 9.5 FR W/OPT INSERT W/O INTRO SHEAT |
Classification | System, Balloon, Intra-aortic And Control |
Applicant | DATASCOPE CORP. 3 FIR CT. P.O. BOX 3100 Oakland, NJ 07436 |
Contact | Robert B Schock |
Correspondent | Robert B Schock 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 | 1990-11-08 |
Decision Date | 1991-06-11 |