FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
EAR CURETTE, VARIOUS
K Number: K841001
·
Decision May 29, 1984
Classifications
1
FEI Numbers
148
Registration Numbers
148
Same Product Code
6
Applicant Total
41
Review Days
81
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Basic Information
- Device Name
- EAR CURETTE, VARIOUS
- K Number
- K841001
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 874.4420
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Applicant
- Premier Dental Products Co.
- Date Received
- March 9, 1984
- Decision Date
- May 29, 1984
- Product Code
- JYG
- Advisory Committee
- Ear, Nose, Throat
- Review Advisory Committee
- EN
- 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 |
|---|---|---|---|
| JYG | Curette, Ear | FDA class 1 | Ear, Nose, Throat |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (JYG), ordered by most recent decision date.
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