Hokanson

FDA UDI

Class II (US FDA UDI)

by D. E. Hokanson, Inc.

Identity

Trade Name: Hokanson FDA UDI
Generic Name: Noninvasive vascular ultrasound system probe FDA UDI
Device Name: DOPPLER PROBE - A complete detachable Doppler probe replacement set. FDA UDI
Model / Reference: MD6 Doppler probe FDA UDI
Description: DOPPLER PROBE - A complete detachable Doppler probe replacement set. FDA UDI

Identifiers

Catalog Number: 01952 FDA UDI
Primary DI / UDI-DI: 00817065021464 FDA UDI
510(k) Number: K901592 FDA UDI
FDA Product Code: DXK FDA UDI
GMDN Term: Noninvasive vascular ultrasound system probe FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.2330 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Noninvasive vascular ultrasound system probe

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

K901592 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 1e60f5e7-bccd-4d9d-b775-b481227a1e0a 36 fields · synced Jun 8, 2026