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

ENSEAL POWERTIP,NSEAL-514D,-525D,-535D,-545D,-514RD,-525RD,-535RD,-545RD, ETRIO-314D,-325D,-335D,-345D, ENSEAL UNIVERSAL

K Number: K081129 · Decision Jul 28, 2008
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
12
Review Days
98

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Basic Information

Device Name
ENSEAL POWERTIP,NSEAL-514D,-525D,-535D,-545D,-514RD,-525RD,-535RD,-545RD, ETRIO-314D,-325D,-335D,-345D, ENSEAL UNIVERSAL
K Number
K081129
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
Surgrx, Inc.
Date Received
April 21, 2008
Decision Date
July 28, 2008
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 Surgrx, Inc.

K Number Device Name
K072493 ENSEAL TISSUE SEALING DEVICE
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K071728 MODIFICATION TO: ENSEAL PTC TISSUE SEALING DEVICE
K070896 ENSEAL PTC TISSUE SEALING DEVICE
K070165 ENSEAL PTC TRIO
K063097 ENSEAL PTC TISSUE SEALING DEVICE
K062949 ENSEAL PTC TISSUE SEATING SEALING DEVICE
K061526 ENSEAL PTC TISSUE SEALING DEVICE
K050671 ENSEAL VESSEL SEALING & HEMOSTASIS SYSTEM
K043008 SURGRX ENSEAL VESSEL SEALING & HEMOSTASIS SYSTEM
Search all 12 clearances from Surgrx, Inc. →