FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
NEEDLE GUIDE MODEL 21285A
K Number: K830753
·
Decision Jun 16, 1983
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
156
Applicant Total
230
Review Days
98
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Basic Information
- Device Name
- NEEDLE GUIDE MODEL 21285A
- K Number
- K830753
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Applicant
- Hewlett-Packard Co.
- Date Received
- March 10, 1983
- Decision Date
- June 16, 1983
- Product Code
- LFL
- Advisory Committee
- Unknown
- 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 |
|---|---|---|---|
| LFL | Instrument, Ultrasonic Surgical | FDA unclassified | Unknown |
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