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

PROOF (BIOLOGICAL/CHEMICAL INDICATOR)

K Number: K801109 · Decision May 30, 1980
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
264
Applicant Total
19
Review Days
18

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Basic Information

Device Name
PROOF (BIOLOGICAL/CHEMICAL INDICATOR)
K Number
K801109
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Amsco Co.
Date Received
May 12, 1980
Decision Date
May 30, 1980
Product Code
JOJ
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
JOJ Indicator, Physical/Chemical Sterilization Process

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Other Clearances by Amsco Co.

K Number Device Name
K912471 EAGLE 3000 SDS
K854922 AMSCO POLARIS SL
K833187 HALL OSTEON
K832945 EAGLE 2000 STERILIZER SERIES GAS/AERA
K832188 HALL RECIPROCATOR
K832187 HALL OSCILLATOR
K831086 CEILING MOUNTED SUPPORT
K832186 HALL DRILL/REAMER
K831309 DELIVERY 4 TABLE
K823360 SURGICAL LIGHT
Search all 19 clearances from Amsco Co. →