The following data is part of a premarket notification filed by Cordis Corporation with the FDA for Saber Percutaneous Transluminal Angioplasty Dilatation Catheter.
Device ID | K133843 |
510k Number | K133843 |
Device Name: | SABER PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILATATION CATHETER |
Classification | Catheter, Angioplasty, Peripheral, Transluminal |
Applicant | CORDIS CORPORATION 6500 PASEO PADRE PKWY Fremont, CA 94555 |
Contact | Kim Fonda |
Correspondent | Kim Fonda CORDIS CORPORATION 6500 PASEO PADRE PKWY Fremont, CA 94555 |
Product Code | LIT |
CFR Regulation Number | 870.1250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-12-18 |
Decision Date | 2014-06-27 |
Summary: | summary |