Identity
- Trade Name
- Vmax FDA UDI
- Generic Name
- Pulmonary function analysis system, adult FDA UDI
- Device Name
- E5550 WIN 7-64 ENG 100-240V JLAB FDA UDI
- Model / Reference
- 29122-507 FDA UDI
- Description
- E5550 WIN 7-64 ENG 100-240V JLAB FDA UDI
Identifiers
- Catalog Number
- 29122-507 FDA UDI
- Primary DI / UDI-DI
- 10190752168244 FDA UDI
- 510(k) Number
- K942211 FDA UDI
- FDA Product Code
- BTY FDA UDI
- GMDN Term
- Pulmonary function analysis system, adult FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1890 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Pulmonary function analysis system, adult
Vmax by Vyaire Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K942211 also covers:
- AVEA — VYAIRE MEDICAL, INC.
- Avea — VYAIRE MEDICAL, INC.
- Avea — VYAIRE MEDICAL, INC.
- FreeFlow™ — VYAIRE MEDICAL, INC.
- VMAX — VYAIRE MEDICAL, INC.
- VMAX — VYAIRE MEDICAL, INC.
- VMAX — VYAIRE MEDICAL, INC.
- VMAX — VYAIRE MEDICAL, INC.
- VMAX — VYAIRE MEDICAL, INC.
- VMAX — VYAIRE MEDICAL, INC.
- VMAX — VYAIRE MEDICAL, INC.
- VMAX — VYAIRE MEDICAL, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Vyaire Medical, Inc.
Sources (1)
- FDA UDI b41fd26c-1844-426e-b57c-8b7c48240cb0 36 fields · synced Jun 7, 2026