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Hokanson

FDA UDI

Class II (US FDA UDI)

by D. E. Hokanson, Inc.

Identity

Trade Name
Hokanson FDA UDI
Generic Name
Blood pressure cuff multichannel valve unit FDA UDI
Device Name
SEGMENTAL CUFF SELECTOR - A pneumatic valve system for interconnecting a cuff inflator to one or multiple blood pressure cuffs. The cuffs can be deflated completely with the valve(s) of the pneumatic valve system, separately from the cuff inflator. FDA UDI
Model / Reference
MV10 FDA UDI
Description
SEGMENTAL CUFF SELECTOR - A pneumatic valve system for interconnecting a cuff inflator to one or multiple blood pressure cuffs. The cuffs can be deflated completely with the valve(s) of the pneumatic valve system, separately from the cuff inflator. FDA UDI

Identifiers

Catalog Number
00387 FDA UDI
Primary DI / UDI-DI
00817065021112 FDA UDI
510(k) Number
K842067 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Blood pressure cuff multichannel valve unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Hokanson by D. E. Hokanson, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K842067 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
D. E. Hokanson, Inc.

Sources (1)

  • FDA UDI 293dda24-c087-4b13-8c38-e2da6a532bcf 37 fields · synced Jun 8, 2026