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Lsp

FDA UDI

Class II (US FDA UDI)

by Allied Medical LLC

Identity

Trade Name
LSP FDA UDI
Generic Name
Airway pressure monitor, powered FDA UDI
Device Name
CPR Timer Assembly FDA UDI
Model / Reference
L770-CPR FDA UDI
Description
CPR Timer Assembly FDA UDI

Identifiers

Catalog Number
L770-CPR FDA UDI
Primary DI / UDI-DI
00026072011539 FDA UDI
510(k) Number
K062080 FDA UDI
FDA Product Code
BTM FDA UDI
GMDN Term
Airway pressure monitor, powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5915 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Airway pressure monitor, powered

Lsp by Allied Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Airway pressure monitor, powered.

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 ba9888ff-8e21-41e5-bcc9-bf8699a16218 35 fields · synced May 30, 2026