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

MONITOR, AERATION, TEC-TEST

K Number: K770953 · Decision Jul 14, 1977
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
205
Applicant Total
21
Review Days
50

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Basic Information

Device Name
MONITOR, AERATION, TEC-TEST
K Number
K770953
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Castle Co.
Date Received
May 25, 1977
Decision Date
July 14, 1977
Product Code
FRC
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
FRC Indicator, Biological Sterilization Process

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K834048 BOVIE CONDUCTIVE ADHES-DISPER-ELECTRO
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
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