510(k) Report

FDA applicant

Beta Biomed Services, Inc.

Crofton, MD2 decisions2001–20020 recalls

FDA records 2 decisions for Beta Biomed Services, Inc. (Crofton, MD) from 2001 to 2002: 2 510(k) clearances. All are in product code DQA (Oximeter). No 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, cardiovascular panel, where it files most

How often FDA has decided Beta Biomed Services, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Beta Biomed Services, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Beta Biomed Services, 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?

  • DQAOximeter2decisions

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K011518Vitalsat SeriesBeta Biomed Services, Inc. · 20021cites it

What has FDA decided for it lately?

  • K011518Vitalsat SeriesBeta Biomed Services, Inc. · 2002
  • K003542Preamp Cable, Model B400-1011PABeta Biomed Services, Inc. · 2001

All 2 as Beta Biomed Services, Inc. →

Other applicant names beginning “Beta”

FDA records each applicant name separately; these may or may not be the same firm.

Beta Bionics, Inc. 9Beta Medical Products Co. 3Beta Labs, Inc. 1Beta Med Pharmaceuticals, Inc. 1Beta Optical Co, Inc. 1Beta Toys, Inc. 1Beta Chemicals, Inc. 1Beta Healthcare Products Pvt., Ltd. 1