FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
AN3100 MULHOLLAND DRAIN
K Number: K872459
·
Decision Jul 21, 1987
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
26
Applicant Total
5
Review Days
28
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Basic Information
- Device Name
- AN3100 MULHOLLAND DRAIN
- K Number
- K872459
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4200
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- H.W. Andersen Products, Inc.
- Date Received
- June 23, 1987
- Decision Date
- July 21, 1987
- Product Code
- GBS
- Advisory Committee
- General, Plastic Surgery
- 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 |
|---|---|---|---|
| GBS | Catheter, Ventricular, General & Plastic Surgery | FDA class 1 | General, Plastic Surgery |
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