The following data is part of a premarket notification filed by Terumo Cardiovascular Systems Corporation with the FDA for Terumo Lauer Lock Adapter.
Device ID | K093992 |
510k Number | K093992 |
Device Name: | TERUMO LAUER LOCK ADAPTER |
Classification | Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass |
Applicant | Terumo Cardiovascular Systems Corporation 125 BLUE BALL RD. Elkton, MD 21921 |
Contact | Eileen Dorsey |
Correspondent | Eileen Dorsey Terumo Cardiovascular Systems Corporation 125 BLUE BALL RD. Elkton, MD 21921 |
Product Code | DTL |
CFR Regulation Number | 870.4290 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-12-24 |
Decision Date | 2010-05-19 |
Summary: | summary |