FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MYELOTEC VIDEO GUIDED CATHETER
K Number: K980734
·
Decision Aug 11, 1998
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
2
Review Days
167
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Basic Information
- Device Name
- MYELOTEC VIDEO GUIDED CATHETER
- K Number
- K980734
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.1100
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Myelotec, Inc.
- Date Received
- February 25, 1998
- Decision Date
- August 11, 1998
- Product Code
- HRX
- Advisory Committee
- Orthopedic
- 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 |
|---|---|---|---|
| HRX | Arthroscope | FDA class 2 | Orthopedic |
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Other Clearances by Myelotec, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K960194 | MYELOTEC MYELOSCOPE | Sep 4, 1996 | Substantially Equivalent |