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

PLASMASEAL OPEN FORCEPS, MODELS 2103PK AND 91701PK

K Number: K061975 · Decision Aug 10, 2006
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
16
Review Days
28

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Basic Information

Device Name
PLASMASEAL OPEN FORCEPS, MODELS 2103PK AND 91701PK
K Number
K061975
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acmi Corporation
Date Received
July 13, 2006
Decision Date
August 10, 2006
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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K052044 ACMI AUTOCLAVABLE URETEROSCOPE, MODELS MR-6A AND MR-6AL
K043581 DUAL LUMEN CATHETER
K042069 INVISIO IRL DIGITAL RIGID LAPAROSCOPE SYSTEM
K042225 ACMI INVISIO ICN, MODELS ICN-0564 AND ICN-0565
K031758 ACMI M4 TELESCOPES
K030960 ECN ELECTRONIC VIDEO CYSTONEPHROSCOPE
K030935 BERKELEY V-10 VACUUM CURETTAGE SYSTEM
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