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Two Channel Electroglottograph EG2-PCX2

FDA UDI

Class II (US FDA UDI)

by Glottal Enterprises, Inc.

Identity

Trade Name
Two Channel Electroglottograph EG2-PCX2 FDA UDI
Generic Name
Electroglottograph FDA UDI
Device Name
Device for the non-invasive measurement of vocal fold contact area. FDA UDI
Model / Reference
EG2-PCX2 FDA UDI
Description
Device for the non-invasive measurement of vocal fold contact area. FDA UDI

Identifiers

Primary DI / UDI-DI
00860011116905 FDA UDI
510(k) Number
K901609 FDA UDI
FDA Product Code
KLX FDA UDI
GMDN Term
Electroglottograph FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1325 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: Electroglottograph

Two Channel Electroglottograph EG2-PCX2 by Glottal Enterprises, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electroglottograph.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 62bcbbce-9e45-4351-9c53-0b7b7b676e0a 34 fields · synced May 30, 2026