510(k) Report

FDA applicant

Center Laboratories, Inc.

Port Washington, NY2 decisions1984–19960 recalls

FDA records 2 decisions for Center Laboratories, Inc. (Port Washington, NY) from 1984 to 1996: 2 510(k) clearances. Most are in product codes BXQ (Rhinoanemometer (Measurement Of Nasal…) and BZH (Meter, Peak Flow, Spirometry). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Center Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Center Laboratories, 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?

  • BXQRhinoanemometer (Measurement Of Nasal Decongestion)1decision
  • BZHMeter, Peak Flow, Spirometry1decision

What has FDA decided for it lately?

  • K954277Astech Peak Flow MeterCenter Laboratories, Inc. · 1996
  • K844230Rhinomanometer A440 DigitalCenter Laboratories, Inc. · 1984

All 2 as Center Laboratories, Inc. →

Other applicant names beginning “Center”

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

Center For Biomaterials and Advanced Technologies 1Center For Marketing Services 1The Center For Craniofacial & Dental Sleep Medicine 1Center For Orthotic and Prosthetic Care,Llc 1Center For Disease Control and Prevention (Cdc) 1