510(k) K851626

SCX-35 THREE CHANNEL ACCESS. FOR MODULE G-2000 ELE by Eaton Medical Group — Product Code DSF

K851626 is an FDA 510(k) premarket notification submitted by Eaton Medical Group for the device "SCX-35 THREE CHANNEL ACCESS. FOR MODULE G-2000 ELE". The FDA issued a decision of Substantially Equivalent on June 26, 1985. The device falls under product code DSF (Recorder, Paper Chart), a Class I device regulated under 21 CFR 870.2810. Eaton Medical Group has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 26, 1985
Date Received
April 18, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Recorder, Paper Chart
Device Class
Class I
Regulation Number
870.2810
Review Panel
CV
Submission Type