The following data is part of a premarket notification filed by Deknatel, Inc. with the FDA for Biosurge(tm) Synchronous Autotrans Procedure Kit.
Device ID | K931106 |
510k Number | K931106 |
Device Name: | BIOSURGE(TM) SYNCHRONOUS AUTOTRANS PROCEDURE KIT |
Classification | Apparatus, Autotransfusion |
Applicant | DEKNATEL, INC. KILOMETER 9 CARRETERA San Jose-heredia, CR |
Contact | Michael Santalucia |
Correspondent | Michael Santalucia DEKNATEL, INC. KILOMETER 9 CARRETERA San Jose-heredia, CR |
Product Code | CAC |
CFR Regulation Number | 868.5830 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-03-03 |
Decision Date | 1993-10-06 |