FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
BIOMONDE LARVAE
K Number: K123449
·
Decision Mar 5, 2013
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
5
Applicant Total
1
Review Days
116
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Basic Information
- Device Name
- BIOMONDE LARVAE
- K Number
- K123449
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Biomonde (A Trading Name of Zoobiotic Limited)
- Date Received
- November 9, 2012
- Decision Date
- March 5, 2013
- Product Code
- NQK
- 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 |
|---|---|---|---|
| NQK | Maggots, Medical | FDA unclassified | Unknown |
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