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

REMANIUM:GM 700, GM 380, GM 800, GFH

K Number: K952867 · Decision Jul 27, 1995
Classifications
1
FEI Numbers
94
Registration Numbers
94
Same Product Code
152
Applicant Total
24
Review Days
35

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Basic Information

Device Name
REMANIUM:GM 700, GM 380, GM 800, GFH
K Number
K952867
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3710
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dentauraum, Inc.
Date Received
June 22, 1995
Decision Date
July 27, 1995
Product Code
EJH
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
EJH Alloy, Metal, Base

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EJH), ordered by most recent decision date.

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Other Clearances by Dentauraum, Inc.

K Number Device Name
K952870 REMANIUM: CS & G-SOFT
K952866 REMATITAN TITANIUM
K952865 REMANIUM: 200,CS, 380, AND CD
K952868 DENTAURUM JACKET CROWN & ROOT POSTS
K942667 DENT-O-CRYL ORTHODONTIC ACRYLIC
K942666 ORTHALGENAT IMPRESSION MATERIAL
K936151 EXTRAORAL HEADGEAR
K942665 ORTHOCENT: LIQUID AND POWDER
K942668 O-TRAY IMPRESSION TRAYS
K935856 DENTAURUM SPACE MAINTAINER
Search all 24 clearances from Dentauraum, Inc. →