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

DELTA

K Number: K945117 · Decision Feb 28, 1997
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
183
Applicant Total
14
Review Days
864

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Basic Information

Device Name
DELTA
K Number
K945117
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6880
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pelton & Crane Co.
Date Received
October 18, 1994
Decision Date
February 28, 1997
Product Code
FLE
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FLE Sterilizer, Steam

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K950299 CEREC 2
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K950030 HELIODENT MD
K936068 ORTHOPHOS 3/ ORTHOPHOS 3C
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K901672 RESUBMITTED WATER PURIFIER FOR USE W/DENTAL TREAT
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