The following data is part of a premarket notification filed by Cas Medical Systems, Inc. with the FDA for Fore-sight, Model Mc-2000 Series (mc 2000, Mc2010, Mc-2020,mc2030).
Device ID | K091452 |
510k Number | K091452 |
Device Name: | FORE-SIGHT, MODEL MC-2000 SERIES (MC 2000, MC2010, MC-2020,MC2030) |
Classification | Oximeter, Tissue Saturation |
Applicant | CAS MEDICAL SYSTEMS, INC. 44 EAST INDUSTRIAL RD. Branford, CT 06405 |
Contact | Ron Jeffrey |
Correspondent | Ron Jeffrey CAS MEDICAL SYSTEMS, INC. 44 EAST INDUSTRIAL RD. Branford, CT 06405 |
Product Code | MUD |
CFR Regulation Number | 870.2700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-05-18 |
Decision Date | 2009-08-21 |
Summary: | summary |