FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

HANSON SCAR ADE

K Number: K040307 · Decision Aug 12, 2004
Classifications
1
FEI Numbers
190
Registration Numbers
190
Same Product Code
80
Applicant Total
14
Review Days
185

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Basic Information

Device Name
HANSON SCAR ADE
K Number
K040307
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4025
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hanson Medical, Inc.
Date Received
February 9, 2004
Decision Date
August 12, 2004
Product Code
MDA
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
MDA Elastomer, Silicone, For Scar Management

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Other Clearances by Hanson Medical, Inc.

K Number Device Name
K141822 SENSEI X ROBOTIC CATHETER SYSTEM
K090803 HANSON MEDICAL FACIAL IMPLANTS
K071018 MONARCH NASAL IMPLANT
K041690 MONARCH NASAL IMPLANT
K030808 HANSON MEDICAL CALF IMPLANT
K030809 HANSON MEDICAL GLUTEAL IMPLANT
K973730 DURASIL I AND DURASIL II
K973729 POWERFLEX PEC IMPLANT
K973573 DURALASTIC ANATOMICAL NASAL IMPLANTS
K973728 SILICONE CARVING BLOCK
Search all 14 clearances from Hanson Medical, Inc. →