3M Laser Imager Xl

by 3M Medical Products Group

510(k) K910092

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

in data synced 22 Oct 2026

Documents

510(k) K910092↗

FDA record

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK910092	Date8 Apr 1991Cleared	StatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K910092
FDA Product Code: LMC

Device Class: Class II
Regulation: 21 CFR Part 892.2040
Advisory Committee: Radiology
FDA Decision: SESE Substantially Equivalent

Other devices from 3M Medical Products Group

Precise Flexistapler Circular Stapler, Series 398X

Class II
Precise Barnd Pi Disposable Surgical Staples

Class II
3M Red Dot 2234 & 2266 Radiolucent Monitoring Electrodes

Class II
3M No Sting Barrier Film

Class I
3M Red Dot 2237 Sticky Gel Monitoring ECG Electrode

Class II
3M Fluid Control System 8300 Cassette Load

Class II

See all devices from 3M Medical Products Group →