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

ORTHOPHOS 3/ ORTHOPHOS 3C

K Number: K936068 · Decision Jul 29, 1994
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
41
Applicant Total
14
Review Days
220

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Basic Information

Device Name
ORTHOPHOS 3/ ORTHOPHOS 3C
K Number
K936068
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1810
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pelton & Crane Co.
Date Received
December 21, 1993
Decision Date
July 29, 1994
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

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

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Other Clearances by Pelton & Crane Co.

K Number Device Name
K972249 ORTHOPHOS PLUS AND ORTHOPHOS PLUS/CD
K972168 SIDEXIS DIGITAL RADIOGRAPHY SYSTEM
K945117 DELTA
K962071 SPIRIT S1/S2
K960819 HELIODENT DS
K950299 CEREC 2
K946187 SPIRIT II AND SPIRIT TREATMENT CENTER
K950030 HELIODENT MD
K935390 SIROLUX FANTASTIC
K901672 RESUBMITTED WATER PURIFIER FOR USE W/DENTAL TREAT
Search all 14 clearances from Pelton & Crane Co. →