FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Greiner Holdex
K Number: K160532
·
Decision Nov 3, 2016
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
5
Review Days
251
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Basic Information
- Device Name
- Greiner Holdex
- K Number
- K160532
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5570
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Greiner Bio-One Na, Inc.
- Date Received
- February 26, 2016
- Decision Date
- November 3, 2016
- Product Code
- FMI
- 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 |
|---|---|---|---|
| FMI | Needle, Hypodermic, Single Lumen | FDA class 2 | General Hospital |
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