FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BR-S601MU (SURGICAL VIDEO RECORDER)
K Number: K890119
·
Decision Jan 24, 1989
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
2
Applicant Total
1
Review Days
13
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Basic Information
- Device Name
- BR-S601MU (SURGICAL VIDEO RECORDER)
- K Number
- K890119
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4160
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Victor Co. of Japan, Ltd. C/O Jvc Corp.
- Date Received
- January 11, 1989
- Decision Date
- January 24, 1989
- Product Code
- FWC
- 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 |
|---|---|---|---|
| FWC | Camera, Television, Surgical, With Audio | FDA class 1 | General, Plastic Surgery |
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