FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ARS ENTERPRISES NEW/REMFR'D GP STEAM STERILIZER 81
K Number: K852113
·
Decision Sep 27, 1985
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
179
Applicant Total
4
Review Days
135
Basic Information
- Device Name
- ARS ENTERPRISES NEW/REMFR'D GP STEAM STERILIZER 81
- K Number
- K852113
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.6880
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- ARS ENTERPRISES, INC.
- Date Received
- May 15, 1985
- Decision Date
- September 27, 1985
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| FLE | Sterilizer, Steam | FDA class 2 | General Hospital |
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