510(k) K891405

BMS-2000 MOBILE EEG SYSTEM by Buckman Co., Inc. — Product Code GYE

K891405 is an FDA 510(k) premarket notification submitted by Buckman Co., Inc. for the device "BMS-2000 MOBILE EEG SYSTEM". The FDA issued a decision of Substantially Equivalent on August 2, 1989. The device falls under product code GYE (Encephalogram Telemetry System), a Class II device regulated under 21 CFR 882.1855. Buckman Co., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 2, 1989
Date Received
March 14, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Encephalogram Telemetry System
Device Class
Class II
Regulation Number
882.1855
Review Panel
NE
Submission Type