Identity
- Trade Name
- Hokanson FDA UDI
- Generic Name
- Foot-switch, electrical FDA UDI
- Device Name
- A manual foot switch used to activate the inflation and deflation of a cuff connected to the E20 Rapid Cuff Inflator. FDA UDI
- Model / Reference
- E20 Foot switch FDA UDI
- Description
- A manual foot switch used to activate the inflation and deflation of a cuff connected to the E20 Rapid Cuff Inflator. FDA UDI
Identifiers
- Catalog Number
- 01800 FDA UDI
- Primary DI / UDI-DI
- 00817065021273 FDA UDI
- 510(k) Number
- K905367 FDA UDI
- FDA Product Code
- DXN FDA UDI
- GMDN Term
- Foot-switch, electrical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1130 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Foot-switch, electrical
Hokanson by D. E. Hokanson, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K905367 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
- D. E. Hokanson, Inc.
Sources (1)
- FDA UDI f4a965f4-4724-4077-87a8-9ee02d2f2f8d 36 fields · synced Jun 8, 2026