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Algo

FDA UDI

Class II (US FDA UDI)

by Natus Medical Incorporated

Identity

Trade Name
ALGO FDA UDI
Generic Name
Evoked-potential audiometer FDA UDI
Device Name
Acoustic Transducer Assembly for ALGO 5. Used to provide acoustic stimulus and monitor ambient noise. FDA UDI
Model / Reference
011120 FDA UDI
Description
Acoustic Transducer Assembly for ALGO 5. Used to provide acoustic stimulus and monitor ambient noise. FDA UDI

Identifiers

Catalog Number
011120 FDA UDI
Primary DI / UDI-DI
00382830043953 FDA UDI
510(k) Number
K073665 FDA UDI
FDA Product Code
GWJ FDA UDI
GMDN Term
Evoked-potential audiometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1900 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Evoked-potential audiometer

Algo by Natus Medical Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Evoked-potential audiometer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c6cca646-2380-42b2-b05e-bf755524f389 36 fields · synced Jun 8, 2026