Skip to content

Moblvac III

by Aeros Instruments, Inc.

510(k) K933902

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

1 ongoing

This device is named in the recall

Documents

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

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK933902 Date20 May 1994ClearedStatusActive

Recalls

1 recall · 1 ongoing · FDA

    • Ongoing Z-0482-2022 FDA Class II initiated 16 Nov 2021

    Increase in premature device failures

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
BTA
Device Class
Class II
Regulation
21 CFR Part 878.4780
Advisory Committee
General, Plastic Surgery
FDA Decision
SESE Substantially Equivalent

Other devices from Aeros Instruments, Inc.

  • Instavac II

    Class II

  • Aeros Aspirator

    Class II

  • Tote-L-Vac

    Class II

  • Care-E-Vac

    Class II