FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ADMS BIOPSY NEEDLE
K Number: K890203
·
Decision Mar 8, 1989
Classifications
1
FEI Numbers
128
Registration Numbers
128
Same Product Code
132
Applicant Total
4
Review Days
50
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Basic Information
- Device Name
- ADMS BIOPSY NEEDLE
- K Number
- K890203
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.1075
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Applicant
- Advanced Diagnostic Medical Systems, Inc.
- Date Received
- January 17, 1989
- Decision Date
- March 8, 1989
- 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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