FDA 510(k)
FDA class 2
Substantially Equivalent
🇬🇧 United Kingdom
MOOR LASER BLOOD FLOW MONITOR MBF3
K Number: K905232
·
Decision Jan 11, 1991
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
13
Review Days
52
Basic Information
- Device Name
- MOOR LASER BLOOD FLOW MONITOR MBF3
- K Number
- K905232
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4810
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- MOOR INSTRUMENTS LTD.
- Date Received
- November 20, 1990
- Decision Date
- January 11, 1991
- Product Code
- GEX
- 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 |
|---|---|---|---|
| GEX | Powered Laser Surgical Instrument | FDA class 2 | General, Plastic Surgery |
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|---|---|---|---|
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| K102433 | MOORVMS-PRES PRESSURE CUFF CONTROLLER | Nov 18, 2010 | Substantially Equivalent |
| K083082 | MOORVMS-LDF1 AND MOORVMS-LDF2 LASER DOPPLER PERFUSION AND TEMPERATURE MONITORS | Jan 13, 2009 | Substantially Equivalent |
| K060976 | MOORLD12-B1 LASER DOPPLER BURNS IMAGER | Mar 27, 2007 | Substantially Equivalent |
| K063586 | MOORFLPI FULL-FIELD LASER PERFUSION IMAGER | Jan 25, 2007 | Substantially Equivalent |
| K063561 | MOORLDLS LASER DOPPLER LINE SCANNER | Jan 19, 2007 | Substantially Equivalent |
| K032841 | MOORLDI INFRARED LASER DOPPLER IMAGER, MODEL MOORLD12-IR | Dec 10, 2003 | Substantially Equivalent |
| K011070 | DRT4 LASER DOPPLER PERFUSION AND TEMPERATURE MONITOR | Nov 7, 2001 | Substantially Equivalent |