The following data is part of a premarket notification filed by American Bentley with the FDA for Hematocrit-saturation Monitor Hsm-100.
Device ID | K852124 |
510k Number | K852124 |
Device Name: | HEMATOCRIT-SATURATION MONITOR HSM-100 |
Classification | Monitor, Blood-gas, On-line, Cardiopulmonary Bypass |
Applicant | AMERICAN BENTLEY P.O. BOX 19522 Irvine, CA 92713 |
Contact | Donald A Raible |
Correspondent | Donald A Raible AMERICAN BENTLEY P.O. BOX 19522 Irvine, CA 92713 |
Product Code | DRY |
CFR Regulation Number | 870.4330 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-05-15 |
Decision Date | 1985-09-16 |