Micro-Touch Nitra Free

by Ansell Healthcare Products LLC

510(k) K092327

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

in data synced 24 Oct 2026

Documents

510(k) K092327↗

FDA record

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Abbreviated	NumberK092327	Date21 Sep 2009Cleared	StatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 24 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K092327
FDA Product Code: LZA
FDA applicant: Ansell Healthcare Products, LLC

Device Class: Class I
Regulation: 21 CFR Part 880.6250
Advisory Committee: General Hospital
FDA Decision: SESE Substantially Equivalent

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