The following data is part of a premarket notification filed by Datascope Corp. with the FDA for Intra Aortic Balloon.
| Device ID | K893243 |
| 510k Number | K893243 |
| Device Name: | INTRA AORTIC BALLOON |
| Classification | System, Balloon, Intra-aortic And Control |
| Applicant | DATASCOPE CORP. 3 FIR CT. P.O. BOX 3100 Oakland, NJ 07436 |
| Contact | Paul Schneider |
| Correspondent | Paul Schneider 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 | 1989-06-01 |
| Decision Date | 1989-06-20 |