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

VOCALIS AND VOCALIS SM

K Number: K081816 · Decision Jan 5, 2009
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
16
Applicant Total
8
Review Days
193

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Basic Information

Device Name
VOCALIS AND VOCALIS SM
K Number
K081816
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cytophil, Inc.
Date Received
June 26, 2008
Decision Date
January 5, 2009
Product Code
MIX
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
MIX System, Vocal Cord Medialization

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Other Clearances by Cytophil, Inc.

K Number Device Name
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K102937 OSTEOPHIL BETA-TCP
K093871 PERIOPHIL B-TCP
K092788 PERIOPHIL BIPHASIC
K081815 VOCALIS GEL
K072219 CYTOPHIL TISSUE MARKER