Identity
- Trade Name
- nSpire Health FDA UDI
- Generic Name
- Diagnostic spirometer, professional FDA UDI
- Device Name
- KoKo Sx 1000 spirometer and software package. The Standalone Edition is configured to operate on a single computer without access to an Iris central database. FDA UDI
- Model / Reference
- KoKo Sx 1000 Diagnostic Spirometer Standalone Edition FDA UDI
- Description
- KoKo Sx 1000 spirometer and software package. The Standalone Edition is configured to operate on a single computer without access to an Iris central database. FDA UDI
Identifiers
- Catalog Number
- 313120 FDA UDI
- Primary DI / UDI-DI
- 00852417003316 FDA UDI
- 510(k) Number
- K914272 FDA UDI
- FDA Product Code
- BZG FDA UDI
- GMDN Term
- Diagnostic spirometer, professional FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1840 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: Diagnostic spirometer, professional
nSpire Health by Nspire Health, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K914272 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
- Nspire Health, Inc.
Sources (1)
- FDA UDI 2ecc32cc-8f9a-4e5d-9e5e-f92bd7f7e314 35 fields · synced Jun 8, 2026