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Complete Controller

FDA UDI

Class II (US FDA UDI)

by Coapt, LLC

Identity

Trade Name
Complete Controller FDA UDI
Generic Name
Myoelectric hand prosthesis FDA UDI
Device Name
Pattern Recognition Processing Unit FDA UDI
Model / Reference
1 FDA UDI
Description
Pattern Recognition Processing Unit FDA UDI

Identifiers

Catalog Number
CC110 FDA UDI
Primary DI / UDI-DI
B618A0 FDA UDI
510(k) Number
K162891 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Myoelectric hand prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 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

No

FDA UDI

Category: Myoelectric hand prosthesis

Complete Controller by Coapt, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Myoelectric hand prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Coapt, LLC

Sources (1)

  • FDA UDI 268bffcf-4850-407d-9b43-fc9061a1040d 35 fields · synced May 31, 2026