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

X-RAY UNIT, DENTAL DIAGNOSTIC

K Number: K760323 · Decision Aug 3, 1976
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
41
Applicant Total
14
Review Days
8

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Basic Information

Device Name
X-RAY UNIT, DENTAL DIAGNOSTIC
K Number
K760323
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1810
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
The S. S. White Co.
Date Received
July 26, 1976
Decision Date
August 3, 1976
Product Code
EAP
Advisory Committee
Dental
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
EAP Unit, X-Ray, Intraoral

Similar 510(k) Clearances

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Other Clearances by The S. S. White Co.

K Number Device Name
K852745 PORCELAIN VENEER SYSTEM BONDING KIT
K852744 CHARACTERIZER KIT VISIBLE LIGHT CURED RESTOR-COLOR
K853005 S.S. WHITE DENTAL X-RAY FILM HOLDER & ALIGNING ARM
K852743 PORCELAIN VENEER SYSTEM LABORATORY KIT
K852182 EASY TRAY & EASY BASE CUSTOM IMPRESSION TRAY MATER
K837440 UNKNOWN
K827816 PODIATRY X-RAY UNIT
K781293 RESTORATIVE SYSTEM PROFILE
K771938 ALGINATE IMPRESSION MATERIAL
K770093 DENTAL BURS
Search all 14 clearances from The S. S. White Co. →