FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Datalys Multi-Parameter Patient Monitor
K Number: K150691
·
Decision May 15, 2015
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
305
Applicant Total
4
Review Days
58
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Basic Information
- Device Name
- Datalys Multi-Parameter Patient Monitor
- K Number
- K150691
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2300
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Lutech Industries, Inc.
- Date Received
- March 18, 2015
- Decision Date
- May 15, 2015
- Product Code
- MWI
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| MWI | Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | FDA class 2 | Cardiovascular |
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