The following data is part of a premarket notification filed by Dideco S.p.a. with the FDA for D731 Micro 20 And D733 Micro 40 Pediatric Arterial Filters.
Device ID | K041061 |
510k Number | K041061 |
Device Name: | D731 MICRO 20 AND D733 MICRO 40 PEDIATRIC ARTERIAL FILTERS |
Classification | Filter, Blood, Cardiopulmonary Bypass, Arterial Line |
Applicant | DIDECO S.P.A. 195 WEST ST. Waltham, MA 02451 -1163 |
Contact | Barry Sall |
Correspondent | Barry Sall DIDECO S.P.A. 195 WEST ST. Waltham, MA 02451 -1163 |
Product Code | DTM |
CFR Regulation Number | 870.4260 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-04-23 |
Decision Date | 2004-05-06 |
Summary: | summary |