FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

SHINMED VARIOUS MODELS OF ELECTRO-SURGICAL PENCILS, SW12200, SW12202, SW12300

K Number: K033027 · Decision Aug 12, 2004
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
4
Review Days
321

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Basic Information

Device Name
SHINMED VARIOUS MODELS OF ELECTRO-SURGICAL PENCILS, SW12200, SW12202, SW12300
K Number
K033027
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shining World Health Care Co., Ltd.
Date Received
September 26, 2003
Decision Date
August 12, 2004
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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K980024 SHINMED MODEL SW-966 ULTRASONIC NEBULIZER