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

MODIFIED CASTLE POWERCLAVE

K Number: K870975 · Decision Apr 17, 1987
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
183
Applicant Total
21
Review Days
38

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Basic Information

Device Name
MODIFIED CASTLE POWERCLAVE
K Number
K870975
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6880
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Castle Co.
Date Received
March 10, 1987
Decision Date
April 17, 1987
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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K833074 CASTLE TEC-TEST S.M.A.R.T. PACK
K831595 CASTLE MODEL 3341 & 3441 & 4141 GAS AER
K792660 1500 EO EXHAUST HOOD
K792649 UNISPORE-BIOLOGICAL INDICATORS
K790677 EO EVACUATING SYSTEM I
K781887 9100 DAYSTAR AND 9110 ORBITER PACKAGE
K781484 CASTLE MODEL 3146 GAS AERATOR
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