510(k) K832883

MINI-PECG by Intersect Systems, Inc. — Product Code DPS

K832883 is an FDA 510(k) premarket notification submitted by Intersect Systems, Inc. for the device "MINI-PECG". The FDA issued a decision of Substantially Equivalent on December 6, 1983. The device falls under product code DPS (Electrocardiograph), a Class II device regulated under 21 CFR 870.2340. Intersect Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 6, 1983
Date Received
August 26, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrocardiograph
Device Class
Class II
Regulation Number
870.2340
Review Panel
CV
Submission Type