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

ARS ENTERPRISES ETHYLENE OXIDE GAS STERILIZER

K Number: K852115 · Decision Nov 1, 1985
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
25
Applicant Total
4
Review Days
170

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Basic Information

Device Name
ARS ENTERPRISES ETHYLENE OXIDE GAS STERILIZER
K Number
K852115
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Ars Enterprises, Inc.
Date Received
May 15, 1985
Decision Date
November 1, 1985
Product Code
FLF
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
FLF Sterilizer, Ethylene-Oxide Gas

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FLF), ordered by most recent decision date.

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Other Clearances by Ars Enterprises, Inc.

K Number Device Name
K852114 ARS ENTERPRISES PRE-VACUUM STEAM STERILIZER 85000
K852113 ARS ENTERPRISES NEW/REMFR'D GP STEAM STERILIZER 81
K831356 STEAM STERILIZER