FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ACE PNEUMATIC OSCILLATING SAW
K Number: K881250
·
Decision Apr 15, 1988
Classifications
1
FEI Numbers
67
Registration Numbers
67
Same Product Code
55
Applicant Total
111
Review Days
23
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Basic Information
- Device Name
- ACE PNEUMATIC OSCILLATING SAW
- K Number
- K881250
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4820
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Buckman Co., Inc.
- Date Received
- March 23, 1988
- Decision Date
- April 15, 1988
- Product Code
- HSZ
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- OR
- 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 |
|---|---|---|---|
| HSZ | Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/Attachment | FDA class 1 | General, Plastic Surgery |
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