510(k) K990788

AD-TECH'S FORAMEN OVALE ELECTRODE by Ad-Tech Medical Instrument Corp — Product Code GZL

K990788 is an FDA 510(k) premarket notification submitted by Ad-Tech Medical Instrument Corp for the device "AD-TECH'S FORAMEN OVALE ELECTRODE". The FDA issued a decision of Substantially Equivalent on November 2, 1999. The device falls under product code GZL (Electrode, Depth), a Class II device regulated under 21 CFR 882.1330. Ad-Tech Medical Instrument Corp has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 2, 1999
Date Received
March 10, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Depth
Device Class
Class II
Regulation Number
882.1330
Review Panel
NE
Submission Type