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

SIROLUX FANTASTIC

K Number: K935390 · Decision Dec 10, 1993
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
22
Applicant Total
14
Review Days
32

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Basic Information

Device Name
SIROLUX FANTASTIC
K Number
K935390
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pelton & Crane Co.
Date Received
November 8, 1993
Decision Date
December 10, 1993
Product Code
EAZ
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
EAZ Light, Operating, Dental

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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
K936068 ORTHOPHOS 3/ ORTHOPHOS 3C
K901672 RESUBMITTED WATER PURIFIER FOR USE W/DENTAL TREAT
Search all 14 clearances from Pelton & Crane Co. →