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CellFX FG5013-01, FG6016-01

by Pulse Biosciences, Inc

CellFX FG5013-01, FG6016-01 (CTT0502) is an electrosurgical system (FDA Class II; FDA product code GEI, Electrosurgical, Cutting & Coagulation & Accessories) made by Pulse Biosciences, Inc, cleared under FDA 510(k) K203299 on 2 Feb 2021 and listed in FDA GUDID since 26 Feb 2021 (UDI-DI 00850003231662), active as of 8 Nov 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 8 Nov 2026

Documents

510(k) K203299

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850003231662 UDI-DI Date26 Feb 2021ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK203299 Date2 Feb 2021DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K203299 decided 2 Feb 2021 Active
  • FDA GUDID UDI-DI 00850003231662 listed 26 Feb 2021 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K203299
  2. Listed FDA GUDID 00850003231662

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
CellFX
Generic name
Electrosurgical system
Model / Ref / Catalog
FG5013-01, FG6016-01, CTT0502
Primary DI / UDI-DI
00850003231662
510(k) Number
FDA product code
GEI
GMDN term
Electrosurgical system
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

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Other devices filed under Electrosurgical system.

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Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)