510(k) K002497

MODEL 4810 ANALYZER OUTPUT ADAPTER by Pace Medical — Product Code DTC

K002497 is an FDA 510(k) premarket notification submitted by Pace Medical for the device "MODEL 4810 ANALYZER OUTPUT ADAPTER". The FDA issued a decision of Substantially Equivalent on October 10, 2000. The device falls under product code DTC (Analyzer, Pacemaker Generator Function), a Class II device regulated under 21 CFR 870.3630. Pace Medical has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 10, 2000
Date Received
August 14, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Analyzer, Pacemaker Generator Function
Device Class
Class II
Regulation Number
870.3630
Review Panel
CV
Submission Type