FDA 510(k) FDA class 3 Unknown 🇺🇸 United States

CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE

K Number: K920822 · Decision Jan 22, 1993
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
7
Review Days
333

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Basic Information

Device Name
CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE
K Number
K920822
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Unknown
Statement or Summary
Summary
Applicant
Siemens-Pacesetter, Inc.
Date Received
February 24, 1992
Decision Date
January 22, 1993
Product Code
DTB
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
DTB Permanent Pacemaker Electrode

Similar 510(k) Clearances

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Other Clearances by Siemens-Pacesetter, Inc.

K Number Device Name
K942440 AFP CARDIAC PACING SYSTEM MODEL 283
K925038 PACING LEAD MODEL 1188T
K932892 PASSIVE PLUS ENDOCARDIAL PACING LEADS VAR. MODELS
K930876 SILICONE BIPOLAR LEAD MODELS 1136T, 1142T &1146T
K925347 MODEL 1148T TRANSVENOUS, SCREW-IN LEAD
K921318 ADAPTING SLEEVE KIT MODEL 4023