FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
BARIREP
K Number: K100839
·
Decision May 11, 2010
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
3
Review Days
48
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Basic Information
- Device Name
- BARIREP
- K Number
- K100839
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Gorbec Pharmaceutical Services, Inc.
- Date Received
- March 24, 2010
- Decision Date
- May 11, 2010
- Product Code
- FRO
- Advisory Committee
- Unknown
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| FRO | Dressing, Wound, Drug | FDA unclassified | Unknown |
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