MODEL 366-10 ADAPTAID STEP-DOWN ADAPTER

Permanent Pacemaker Electrode

INTERMEDICS, INC.

The following data is part of a premarket notification filed by Intermedics, Inc. with the FDA for Model 366-10 Adaptaid Step-down Adapter.

Pre-market Notification Details

Device IDK861110
510k NumberK861110
Device Name:MODEL 366-10 ADAPTAID STEP-DOWN ADAPTER
ClassificationPermanent Pacemaker Electrode
Applicant INTERMEDICS, INC. P.O. BOX 617 Freeport,  TX  77541 -0617
ContactKen Bishop
CorrespondentKen Bishop
INTERMEDICS, INC. P.O. BOX 617 Freeport,  TX  77541 -0617
Product CodeDTB  
CFR Regulation Number870.3680 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-03-25
Decision Date1986-04-23

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.