FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
REDI-DRAPE
K Number: K830723
·
Decision Apr 12, 1983
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
3
Review Days
35
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Basic Information
- Device Name
- REDI-DRAPE
- K Number
- K830723
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4370
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- The Oec Group
- Date Received
- March 8, 1983
- Decision Date
- April 12, 1983
- Product Code
- KKX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| KKX | Drape, Surgical, Antimicrobial | FDA class 2 | General, Plastic Surgery |
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