FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HIGH TORQUE TEMPORARY PERVENOUS LEAD W/DEPTH MARK

K Number: K882045 · Decision Jul 12, 1988
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
128
Applicant Total
4
Review Days
57

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Basic Information

Device Name
HIGH TORQUE TEMPORARY PERVENOUS LEAD W/DEPTH MARK
K Number
K882045
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Cordis Leads, Inc.
Date Received
May 16, 1988
Decision Date
July 12, 1988
Product Code
LDF
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LDF Electrode, Pacemaker, Temporary

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LDF), ordered by most recent decision date.

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Other Clearances by Cordis Leads, Inc.

K Number Device Name
K883070 ENCOR UNIPOLAR VS-1 LEADS
K873772 CHANGES TO ENCOR PERVENOUS J-ATRIAL LEADS
K874366 ENCOR BIPOLAR ACT/FIXA LEAD W/POR SUR ELE #329-201