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Life Support Products (LSP)

FDA UDI

Class II (US FDA UDI)

by Allied Medical LLC

Identity

Trade Name
Life Support Products (LSP) FDA UDI
Generic Name
Demand valve FDA UDI
Device Name
Demand Valve, W/O Hose, ISO. FDA UDI
Model / Reference
L324-020I FDA UDI
Description
Demand Valve, W/O Hose, ISO. FDA UDI

Identifiers

Catalog Number
L324-020-I FDA UDI
Primary DI / UDI-DI
00026072000748 FDA UDI
510(k) Number
K915564 FDA UDI
FDA Product Code
BTL FDA UDI
GMDN Term
Demand valve FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5925 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

Yes

FDA UDI

Category: Demand valve

Life Support Products (LSP) by Allied Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Demand valve.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allied Medical LLC

Sources (1)

  • FDA UDI 90be7e67-3d83-437e-a82e-3d65fda6f417 35 fields · synced May 30, 2026