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

SILICONE CARVING BLOCK

K Number: K973728 · Decision Nov 13, 1997
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
44
Applicant Total
14
Review Days
44

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Basic Information

Device Name
SILICONE CARVING BLOCK
K Number
K973728
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hanson Medical, Inc.
Date Received
September 30, 1997
Decision Date
November 13, 1997
Product Code
MIB
Advisory Committee
Ear, Nose, Throat
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
MIB Elastomer, Silicone Block

Similar 510(k) Clearances

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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
K040307 HANSON SCAR ADE
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
Search all 14 clearances from Hanson Medical, Inc. →