510(k) K781327

Device
Pulse Generator, Model 240, External
Applicant
INTERMEDICS, INC.
510(k) number
K781327
Product code
DTE
Decision
Substantially Equivalent (SESE)
Decision date
1978-12-11
Date received
1978-08-01
Regulation
870.3600
Classification name
Pulse-Generator, Pacemaker, External
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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510(k), Device, Applicant table
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