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Footpedal, M2000, MTP

FDA UDI

Class II (US FDA UDI)

by Medical Technical Products, Inc

Identity

Trade Name
Footpedal, M2000, MTP FDA UDI
Generic Name
Foot-switch, electrical FDA UDI
Model / Reference
48-9210 FDA UDI

Identifiers

Primary DI / UDI-DI
00850039020049 FDA UDI
510(k) Number
K940084 FDA UDI
FDA Product Code
HQC FDA UDI
GMDN Term
Foot-switch, electrical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4670 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

Footpedal, M2000, MTP by Medical Technical Products, 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

Sources (1)

  • FDA UDI c211e291-a260-403a-9852-80dfd1574c74 34 fields · synced Jun 6, 2026