510(k) K951226

VITALMAX 4000/MINIPACK 3100/3000 by Pace Tech, Inc. — Product Code DSK

K951226 is an FDA 510(k) premarket notification submitted by Pace Tech, Inc. for the device "VITALMAX 4000/MINIPACK 3100/3000". The FDA issued a decision of Substantially Equivalent on November 21, 1996. The device falls under product code DSK (Computer, Blood-Pressure), a Class II device regulated under 21 CFR 870.1110. Pace Tech, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 21, 1996
Date Received
March 20, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Computer, Blood-Pressure
Device Class
Class II
Regulation Number
870.1110
Review Panel
CV
Submission Type