FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MDT CHEMITEST SEE-THRU BAG
K Number: K831425
·
Decision Jun 2, 1983
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
1
Review Days
30
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Basic Information
- Device Name
- MDT CHEMITEST SEE-THRU BAG
- K Number
- K831425
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.6850
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Kenpak Converters, Inc.
- Date Received
- May 3, 1983
- Decision Date
- June 2, 1983
- Product Code
- FRG
- 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 |
|---|---|---|---|
| FRG | Wrap, Sterilization | FDA class 2 | General Hospital |
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