FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
STAYFREE, UNSCENTED/SCENTED/SCENTED DEODOR MEN PAD
K Number: K911637
·
Decision Aug 2, 1991
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
2
Applicant Total
45
Review Days
113
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Basic Information
- Device Name
- STAYFREE, UNSCENTED/SCENTED/SCENTED DEODOR MEN PAD
- K Number
- K911637
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.4845
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Personal Products Co.
- Date Received
- April 11, 1991
- Decision Date
- August 2, 1991
- Product Code
- HAD
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| HAD | Rongeur, Powered | FDA class 2 | Neurology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (HAD), ordered by most recent decision date.
AESCULAP PNEUMATIC KERRISON
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ANSPACH POWERED KERRISON SYSTEM (PKS)
FDA 510(k)
FDA Class 2
·Neurology
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