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

Renu Gel

K Number: K150400 · Decision Apr 6, 2015
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
16
Applicant Total
8
Review Days
47

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Basic Information

Device Name
Renu Gel
K Number
K150400
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cytophil, Inc.
Date Received
February 18, 2015
Decision Date
April 6, 2015
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
K121795 CALCIUM HYDROXYLAPATITE VOCAL FOLD IMPLANT
K102937 OSTEOPHIL BETA-TCP
K093871 PERIOPHIL B-TCP
K092788 PERIOPHIL BIPHASIC
K081815 VOCALIS GEL
K081816 VOCALIS AND VOCALIS SM
K072219 CYTOPHIL TISSUE MARKER