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

SURGICAL TROCAR

K Number: K911462 · Decision Apr 22, 1991
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
50
Applicant Total
14
Review Days
19

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Basic Information

Device Name
SURGICAL TROCAR
K Number
K911462
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1390
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Applied Medical
Date Received
April 3, 1991
Decision Date
April 22, 1991
Product Code
DRC
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DRC Trocar

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