FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
INNOMED PD-1 KIT
K Number: K822574
·
Decision Oct 13, 1982
Classifications
1
FEI Numbers
47
Registration Numbers
48
Same Product Code
10
Applicant Total
3
Review Days
50
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Basic Information
- Device Name
- INNOMED PD-1 KIT
- K Number
- K822574
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.5960
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Innomed Corp.
- Date Received
- August 24, 1982
- Decision Date
- October 13, 1982
- Product Code
- LJL
- Advisory Committee
- General Hospital
- 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 |
|---|---|---|---|
| LJL | Detectors And Removers, Lice, (Including Combs) | FDA class 1 | General Hospital |
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