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

EMC MODEL STATOME 200

K Number: K952231 · Decision Nov 21, 1995
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
3
Review Days
193

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Basic Information

Device Name
EMC MODEL STATOME 200
K Number
K952231
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Emc Industries
Date Received
May 12, 1995
Decision Date
November 21, 1995
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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Other Clearances by Emc Industries

K Number Device Name
K941721 EMC MODEL NO. 322870 ENDOSTAT
K911353 EMC MODEL NO. STATOME 900