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

SANARUS INDICA MARKER SYSTEM

K Number: K020054 · Decision Oct 16, 2002
Classifications
1
FEI Numbers
112
Registration Numbers
112
Same Product Code
175
Applicant Total
14
Review Days
281

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Basic Information

Device Name
SANARUS INDICA MARKER SYSTEM
K Number
K020054
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sanarus Medical, Inc.
Date Received
January 8, 2002
Decision Date
October 16, 2002
Product Code
FZP
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FZP Clip, Implantable

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Other Clearances by Sanarus Medical, Inc.

K Number Device Name
K080171 SANARUS INCORE ROTATIONAL CORE BIOPSY DEVICE, MODELS CB3010, CB3012
K073533 SANARUS V2 TREATMENT SYSTEM
K062896 V2 TREATMENT SYSTEM (V2 CONSOLE, V2 ICE PROBE, V2 DEWARS) MODELS; VS3000, VP0600, VD0600
K061510 SANARUS VISICA TREATMENT SYSTEM
K052861 MODIFICATION TO:SANARUS VISICA TREATMENT SYSTEM , MODELS VS2000
K051581 SANARUS CASSI II ROTATIONAL CORE BIOPSY SYSTEM, MODEL CS2000
K042136 SANARUS CASSI ROTATIONAL CORE BIOPSY SYSTEM
K032506 SANARUS CENTRICA II ROTATIONAL CORE BIOPSY SYSTEM
K022314 SANARUS VISICA TREATMENT SYSTEM
K022879 MODIFICATION TO SANARUS CENTRICA CORE TISSUE BIOPSY
Search all 14 clearances from Sanarus Medical, Inc. →