Phasor 4.50K

by Phasor Health, LLC

Phasor 4.50K is a Class II device made by Phasor Health, LLC, listed in FDA GUDID since 16 Feb 2023 (UDI-DI B775450K0), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberB775450K0 UDI-DI	Date16 Feb 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Phasor
Generic name: Automatic cranial perforator, single-use
Model / Ref / Catalog: 4.50K

Primary DI / UDI-DI: B775450K0
FDA product code: HBE
GMDN term: Automatic cranial perforator, single-use

Device class: Class II
Regulation number: 882.4310
GUDID distribution status: In Commercial Distribution

MRI safety: MR Unsafe

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Properties

Supplied sterile
Single use
Prescription use
Convenience kit
Lot / batch number
Expiration date
Manufacturing date

Other properties (8, all answered No)