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Double pedal foot switch PZ300

by W.O.M. World of Medicine GmbH

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04056702011994 UDI-DI Date10 Mar 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Double pedal foot switch
Generic Name
Foot-switch, electrical
Model / Ref / Catalog
PZ300, 284228
Primary DI / UDI-DI
04056702011994
510(k) Number
FDA Product Code
HRX
GMDN Term
Foot-switch, electrical
Device Class
Class II
Regulation Number
888.1100
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K250795)

Show all (9)

Other devices from W.O.M. World of Medicine GmbH

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Properties

  • Lot / Batch Number
  • Manufacturing Date

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No