FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DURATECH HOSPITAL TOWEL
K Number: K920045
·
Decision Jul 2, 1992
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
3
Review Days
178
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Basic Information
- Device Name
- DURATECH HOSPITAL TOWEL
- K Number
- K920045
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4370
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Techstyles
- Date Received
- January 6, 1992
- Decision Date
- July 2, 1992
- 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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