510(k) K810016

REPLACABLE BATTERY PERFECTEMP CAUTERY by Medical Products Development, Inc. — Product Code HQP

K810016 is an FDA 510(k) premarket notification submitted by Medical Products Development, Inc. for the device "REPLACABLE BATTERY PERFECTEMP CAUTERY". The FDA issued a decision of Substantially Equivalent on April 23, 1981. The device falls under product code HQP (Unit, Cautery, Thermal, Battery-Powered), a Class II device regulated under 21 CFR 886.4115. Medical Products Development, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 23, 1981
Date Received
January 5, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Unit, Cautery, Thermal, Battery-Powered
Device Class
Class II
Regulation Number
886.4115
Review Panel
OP
Submission Type