FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GILLETTE CORDLESS WHIRLPOOL
K Number: K791603
·
Decision Sep 7, 1979
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
72
Applicant Total
3
Review Days
24
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Basic Information
- Device Name
- GILLETTE CORDLESS WHIRLPOOL
- K Number
- K791603
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.5100
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Applicant
- The Gillette Company
- Date Received
- August 14, 1979
- Decision Date
- September 7, 1979
- Product Code
- ILJ
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| ILJ | Bath, Hydro-Massage | FDA class 2 | Physical Medicine |
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