510(k) Report

FDA applicant

Aeros Instruments, Inc.

Northbrook, IL5 decisions1993–19951 recall

FDA records 5 decisions for Aeros Instruments, Inc. (Northbrook, IL) from 1993 to 1995: 5 510(k) clearances. All are in product code BTA (Pump, Portable, Aspiration (Manual Or Powered)). 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Aeros Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aeros Instruments, Inc. since 2007.

Recalls per year

1in 2021

2021: 1
2007high 1 (2021) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Aeros Instruments, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • BTAPump, Portable, Aspiration (Manual Or Powered)5decisions

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K933902Moblvac IiiAeros Instruments, Inc. · 19941cites it
  • K926566Care-E-VacAeros Instruments, Inc. · 19931cites it

What has FDA decided for it lately?

  • K952103Aeros AspiratorAeros Instruments, Inc. · 1995
  • K933902Moblvac IiiAeros Instruments, Inc. · 19941 recall
  • K934976Instavac IIAeros Instruments, Inc. · 1994
  • K932051Tote-L-VacAeros Instruments, Inc. · 1993
  • K926566Care-E-VacAeros Instruments, Inc. · 1993

All 5 as Aeros Instruments, Inc. →

What has been recalled?

1 recall linked to its devices; the latest:

  • K933902Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and…Nov 16, 2021Class II