FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇰 Denmark
°M Warmer System
K Number: K232107
·
Decision May 31, 2024
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
74
Applicant Total
2
Review Days
322
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Basic Information
- Device Name
- °M Warmer System
- K Number
- K232107
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5725
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Mequ A/S
- Date Received
- July 14, 2023
- Decision Date
- May 31, 2024
- Product Code
- LGZ
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| LGZ | Warmer, Thermal, Infusion Fluid | FDA class 2 | General Hospital |
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Other Clearances by Mequ A/S
| K Number | Device Name | ||
|---|---|---|---|
| K260988 | °M Warmer System with °M Station | Apr 24, 2026 | Substantially Equivalent |