Identity
- Trade Name
- KoKo FDA UDI
- Generic Name
- Monitoring spirometer, mechanical FDA UDI
- Device Name
- Wright Respirometer Mk 14 FDA UDI
- Model / Reference
- Wright Respirometer Mk 14 FDA UDI
- Description
- Wright Respirometer Mk 14 FDA UDI
Identifiers
- Catalog Number
- 700-014 FDA UDI
- Primary DI / UDI-DI
- 05065016557011 FDA UDI
- 510(k) Number
- K091853 FDA UDI
- FDA Product Code
- BZK FDA UDI
- GMDN Term
- Monitoring spirometer, mechanical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1850 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
Yes
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
No
FDA UDI
Category: Monitoring spirometer, mechanical
KoKo by Koko Pft Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K091853 also covers:
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
- Koko Pft Ltd
Sources (1)
- FDA UDI 567d5936-1c10-4e29-8673-22bc1873e81c 35 fields · synced May 30, 2026