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Pioneer Pro Wired Footswitch

FDA UDI

Class II (US FDA UDI)

by Cao Group, Inc.

Identity

Trade Name
Pioneer Pro Wired Footswitch FDA UDI
Generic Name
Foot-switch, electrical FDA UDI
Device Name
Wired footswitch for use with the Pioneer Pro Diode Laser. FDA UDI
Model / Reference
002-00307 FDA UDI
Description
Wired footswitch for use with the Pioneer Pro Diode Laser. FDA UDI

Identifiers

Catalog Number
002-00307 FDA UDI
Primary DI / UDI-DI
00872320003265 FDA UDI
510(k) Number
K062619 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Foot-switch, electrical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

Yes

FDA UDI

Category: Foot-switch, electrical

Pioneer Pro Wired Footswitch by Cao Group, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foot-switch, electrical.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cao Group, Inc.

Sources (1)

  • FDA UDI 01a37a0d-88eb-4179-90e0-bbea30309b28 36 fields · synced May 31, 2026