FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
HYDRASORB(TM)
K Number: K897156
·
Decision Feb 21, 1990
Classifications
1
FEI Numbers
502
Registration Numbers
502
Same Product Code
106
Applicant Total
4
Review Days
57
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Basic Information
- Device Name
- HYDRASORB(TM)
- K Number
- K897156
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4020
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Avitar, Inc.
- Date Received
- December 26, 1989
- Decision Date
- February 21, 1990
- Product Code
- NAD
- 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 |
|---|---|---|---|
| NAD | Dressing, Wound, Occlusive | FDA class 1 | General, Plastic Surgery |
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