FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CASPAR SCALP CLIP, APPLIER
K Number: K890443
·
Decision Jun 15, 1989
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
9
Applicant Total
13
Review Days
139
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Basic Information
- Device Name
- CASPAR SCALP CLIP, APPLIER
- K Number
- K890443
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.4150
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Aesculap Instruments Corp.
- Date Received
- January 27, 1989
- Decision Date
- June 15, 1989
- Product Code
- HBO
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| HBO | Clip, Scalp | FDA class 2 | Neurology |
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