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

FILE, PULP CANAL

K Number: K800293 · Decision Feb 19, 1980
Classifications
1
FEI Numbers
160
Registration Numbers
160
Same Product Code
30
Applicant Total
23
Review Days
8

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Basic Information

Device Name
FILE, PULP CANAL
K Number
K800293
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Ipco Corp.
Date Received
February 11, 1980
Decision Date
February 19, 1980
Product Code
EKS
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
EKS File, Pulp Canal, Endodontic

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K871270 PERFORM DENTURE BASE RESIN
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K850906 TACTILE PLUS DENTAL ELEVATORS
K842836 SAFE & SOFT MINI PADS & MAXI PADS
K842837 SAFE & SOFT MAXI SHILEDS
K842838 SAFE & SOFT PANTY SHIELDS
K841953 ULTRA SHIELD BRIEFS
K840753 AMBEZE DISPOSABLE INCONTINENCE PANTS
K840754 MAXISHIELD INCONTINENCE CARE SYSTEM
K840755 MINIGARD DISPOSABLE LINERS
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