FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DUKAL N95PARTICULATE RESPIRATOR/SURGICAL FACE MASK
K Number: K070692
·
Decision May 30, 2007
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
34
Applicant Total
2
Review Days
78
Basic Information
- Device Name
- DUKAL N95PARTICULATE RESPIRATOR/SURGICAL FACE MASK
- K Number
- K070692
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4040
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- DUKAL CORPORATION
- Date Received
- March 13, 2007
- Decision Date
- May 30, 2007
- Product Code
- MSH
- 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 |
|---|---|---|---|
| MSH | Respirator, Surgical | FDA class 2 | General, Plastic Surgery |
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Other Clearances by DUKAL CORPORATION
| K Number | Device Name | ||
|---|---|---|---|
| K113689 | DUKAL LUBRICATING JELLY | May 4, 2012 | Substantially Equivalent |