Identity
- Trade Name
- PFM FDA UDI
- Generic Name
- Peak flow meter, manual FDA UDI
- Device Name
- 4300 PEAK FLOW METER GERMAN FDA UDI
- Model / Reference
- 4300 FDA UDI
- Description
- 4300 PEAK FLOW METER GERMAN FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05099169434004 FDA UDI
- 510(k) Number
- K781922 FDA UDI
- FDA Product Code
- BZH FDA UDI
- GMDN Term
- Peak flow meter, manual FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1860 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Peak flow meter, manual
Pfm by Vitalograph Ireland, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K781922 also covers:
- PFM — Vitalograph Ireland, Ltd.
- PFM — Vitalograph Ireland, Ltd.
- PFM — Vitalograph Ireland, Ltd.
- PFM — Vitalograph Ireland, Ltd.
- PFM — Vitalograph Ireland, Ltd.
- PFM — Vitalograph Ireland, Ltd.
- PFM — Vitalograph Ireland, Ltd.
- PFM — Vitalograph Ireland, Ltd.
- PFM — Vitalograph Ireland, Ltd.
- PFM — Vitalograph Ireland, Ltd.
- PFM — Vitalograph Ireland, Ltd.
- PFM — Vitalograph Ireland, Ltd.
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
- Vitalograph Ireland, Ltd.
Sources (1)
- FDA UDI 52cdc40e-8ad5-41f8-856c-b7d2ec2ba97b 35 fields · synced May 30, 2026