FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ACE/KYLE SELF TAPPING CANNULATED TITA

K Number: K833866 · Decision Dec 27, 1983
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
0
Applicant Total
111
Review Days
50

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Basic Information

Device Name
ACE/KYLE SELF TAPPING CANNULATED TITA
K Number
K833866
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.5220
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Buckman Co., Inc.
Date Received
November 7, 1983
Decision Date
December 27, 1983
Product Code
JPW
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
JPW Pump, Nebulizer, Electrically Powered

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