Skip to content

PowerWire 14 Radiofrequency Guidewire Kit PW14-190-20A

by Baylis Medical Technologies Inc

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 Number07540299000471 UDI-DI Date4 Dec 2025ListedStatusListed 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  • Withdrawn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
PowerWire 14 Radiofrequency Guidewire Kit
Generic Name
Endoscopic electrosurgical electrode, monopolar, single-use
Model / Reference
PW14-190-20A
Primary DI / UDI-DI
07540299000471
510(k) Number
FDA Product Code
PDU, DSA
GMDN Term
Endoscopic electrosurgical electrode, monopolar, single-use
Device Class
Class II
Regulation Number
870.1250, 870.2900
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K251158)

Other devices from Baylis Medical Technologies Inc

See all devices from Baylis Medical Technologies Inc →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No