FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
DEBRISAN (DEXTRANOMER) PASTE
K Number: K800737
·
Decision Aug 4, 1980
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
21
Applicant Total
5
Review Days
124
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Basic Information
- Device Name
- DEBRISAN (DEXTRANOMER) PASTE
- K Number
- K800737
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4018
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Pharmaseal Laboratories
- Date Received
- April 2, 1980
- Decision Date
- August 4, 1980
- Product Code
- KOZ
- 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 |
|---|---|---|---|
| KOZ | Beads, Hydrophilic, For Wound Exudate Absorption | FDA class 1 | General, Plastic Surgery |
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