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

EAR APPLICATOR, CATALOG NO. 2229

K Number: K870762 · Decision Mar 6, 1987
Classifications
1
FEI Numbers
364
Registration Numbers
364
Same Product Code
20
Applicant Total
80
Review Days
8

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Basic Information

Device Name
EAR APPLICATOR, CATALOG NO. 2229
K Number
K870762
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Treace Medical, Inc.
Date Received
February 26, 1987
Decision Date
March 6, 1987
Product Code
KXF
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KXF Applicator, Absorbent Tipped, Non-Sterile

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Other Clearances by Treace Medical, Inc.

K Number Device Name
K883727 BUCKET PROSTHESIS PORP
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K874779 BIPOLATOR 50
K873154 TREACE MAGNUM OTO-TOOL SYSTEM
K872000 EYE GARD
K870765 CANNULATED INSTRUMENT CLEANERS
K871706 OPTHA PREP
K870759 CLEANING SOLUTION, CATALOG NO. 8203
K870766 PROSTHESIS WIRE
K870760 BUR BRUSH
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