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Du-O-Vac

FDA UDI

Class II (US FDA UDI)

by W.t. Farley, Inc.

Identity

Trade Name
Du-O-Vac FDA UDI
Generic Name
Emergency airway clearance suction system, pneumatic FDA UDI
Device Name
Emergency Venturi Suction Device FDA UDI
Model / Reference
MRI-DV-5142 FDA UDI
Description
Emergency Venturi Suction Device FDA UDI

Identifiers

Primary DI / UDI-DI
00856438007643 FDA UDI
510(k) Number
K781988 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Emergency airway clearance suction system, pneumatic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Pressure — 50 Pound per Square Inch FDA UDI

Category: Emergency airway clearance suction system, pneumatic

Du-O-Vac by W.t. Farley, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Emergency airway clearance suction system, pneumatic.

Cleared under the same submission

K781988 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
W.t. Farley, Inc.

Sources (1)

  • FDA UDI efd8b485-af85-4f33-87f3-6d62ba887171 35 fields · synced May 30, 2026