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460p

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
460P FDA UDI
Generic Name
Camera control unit FDA UDI
Device Name
CAMERA CONTROL UNIT PAL 460P FDA UDI
Model / Reference
72200088 FDA UDI
Description
CAMERA CONTROL UNIT PAL 460P FDA UDI

Identifiers

Catalog Number
72200088 FDA UDI
Primary DI / UDI-DI
03596010539359 FDA UDI
510(k) Number
K031379 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Camera control unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Camera control unit

460p by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Camera control unit.

Cleared under the same submission

K031379 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 93832314-a7f8-45d2-9164-8ae7c14cc776 36 fields · synced Jun 8, 2026