FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

HARMONIC ACE CURVED SHEARS WITH HAND CONTROL, MODEL ACE23P, ACE36P

K Number: K042777 · Decision Dec 1, 2004
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
156
Applicant Total
111
Review Days
56

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Basic Information

Device Name
HARMONIC ACE CURVED SHEARS WITH HAND CONTROL, MODEL ACE23P, ACE36P
K Number
K042777
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ethicon Endo-Surgery, Inc.
Date Received
October 6, 2004
Decision Date
December 1, 2004
Product Code
LFL
Advisory Committee
Unknown
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
LFL Instrument, Ultrasonic Surgical

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K102632 ETHICON ENDO-SURGERY 5MM LAPAROSCOPIC MULTI-FEED STAPLER
K093896 ETHICON ENDO SURGERY SLOTTED ANOSCOPE
K091259 ETHICON ENDO-SURGERY FLEXIBLE BIPOLAR HEMOSTASIS FORCEPS
K091824 ETHICON ENDO-SURGERY ROTATING ENDOSCOPIC SCISSORS, MODEL IN2507
K093236 ETHICON ENDO-SURGERYOPTICAL DILATOR
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Search all 111 clearances from Ethicon Endo-Surgery, Inc. →