FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ACU-CURETTE
K Number: K891334
·
Decision Apr 11, 1989
Classifications
1
FEI Numbers
216
Registration Numbers
216
Same Product Code
13
Applicant Total
13
Review Days
32
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Basic Information
- Device Name
- ACU-CURETTE
- K Number
- K891334
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4800
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Acuderm, Inc.
- Date Received
- March 10, 1989
- Decision Date
- April 11, 1989
- Product Code
- FZS
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| FZS | Curette, Surgical, General Use | FDA class 1 | General, Plastic Surgery |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (FZS), ordered by most recent decision date.
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ADENOID CURETTE
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MICRODISCECTOMY CURETTE SET
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Other Clearances by Acuderm, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K933516 | ACU-E PUNCH | Mar 24, 1994 | Substantially Equivalent |
| K933265 | ACU-DISPO-CE(TM) | Mar 7, 1994 | Substantially Equivalent |
| K933137 | ACU-SUTURE KIT | Feb 22, 1994 | Substantially Equivalent |
| K930043 | ACU-EVAC | Feb 9, 1994 | Substantially Equivalent |
| K933866 | ACU-HEMOSTATIC RING | Dec 1, 1993 | Substantially Equivalent |
| K915000 | ACU-GUARD | Jan 27, 1992 | Substantially Equivalent |
| K874024 | ACU-MICRO-NEEDLE | Nov 23, 1987 | Substantially Equivalent |
| K854877 | ACU-SYRINGE W/WO NEEDLES | Feb 19, 1986 | Substantially Equivalent |
| K832582 | MYCOSEL AGAR | Sep 12, 1983 | Substantially Equivalent |
| K832583 | SABOURAUD DEXTROSE AGAR | Sep 12, 1983 | Substantially Equivalent |