FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
THYROSAMPLER
K Number: K062979
·
Decision May 30, 2007
Classifications
1
FEI Numbers
128
Registration Numbers
128
Same Product Code
132
Applicant Total
1
Review Days
243
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Basic Information
- Device Name
- THYROSAMPLER
- K Number
- K062979
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.1075
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Acd Medical Innovation Corp.
- Date Received
- September 29, 2006
- Decision Date
- May 30, 2007
- Product Code
- FCG
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- GU
- 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 |
|---|---|---|---|
| FCG | Biopsy Needle | FDA class 2 | Gastroenterology, Urology |
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