The following data is part of a premarket notification filed by Solco Basle, Inc. with the FDA for Solcotrans Intraoperative Autotransfusion System.
Device ID | K896858 |
510k Number | K896858 |
Device Name: | SOLCOTRANS INTRAOPERATIVE AUTOTRANSFUSION SYSTEM |
Classification | Apparatus, Autotransfusion |
Applicant | SOLCO BASLE, INC. 72 SHARP ST. HINGHAM CORPORATE CTR. Hingham, MA 02043 |
Contact | Barbara Lambert |
Correspondent | Barbara Lambert SOLCO BASLE, INC. 72 SHARP ST. HINGHAM CORPORATE CTR. Hingham, MA 02043 |
Product Code | CAC |
CFR Regulation Number | 868.5830 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-12-05 |
Decision Date | 1990-04-05 |