510(k) K812608

VASCULAB #R12B by Medasonics, Inc. — Product Code DSF

K812608 is an FDA 510(k) premarket notification submitted by Medasonics, Inc. for the device "VASCULAB #R12B". The FDA issued a decision of Substantially Equivalent on October 2, 1981. The device falls under product code DSF (Recorder, Paper Chart), a Class I device regulated under 21 CFR 870.2810. Medasonics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 2, 1981
Date Received
September 15, 1981
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