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Spirometer, Diagnostic

FDA product code BZG · Class 2 · Anesthesiology

1,162
Registered devices
31
Adverse events
1
Recalls
228
510(k) clearances

Devices with this code

Vyaire — Jaeger Medical GmbHWelch Allyn, Inc. — WELCH ALLYN, INC.Polytech Filter — POLYTECHNIC RESOURCES INCFloSense II — S D I DIAGNOSTICS INCMouthpiece — VITALOGRAPH (IRELAND) LIMITEDPolytech Filter — POLYTECHNIC RESOURCES INCPolytech Filter — POLYTECHNIC RESOURCES INCPneumotrac — VITALOGRAPH (IRELAND) LIMITEDPolytech Filter — POLYTECHNIC RESOURCES INCAstra Spirometer — S D I DIAGNOSTICS INCAlpha — VITALOGRAPH (IRELAND) LIMITEDVyaire — Jaeger Medical GmbHCuraplex — TRI-ANIM HEALTH SERVICES, INC.PFT — VITALOGRAPH (IRELAND) LIMITEDPulmonary Filtration Technologies — WHITE CARDIOPULMONARY, INC.Astra Spirometer — S D I DIAGNOSTICS INCAlpha — VITALOGRAPH (IRELAND) LIMITEDWelch Allyn, Inc. — WELCH ALLYN, INC.M915-PCD, PCD Spirometer Kit — Medikro OySpiro PD — PMD HEALTHCARE, INC.DISPIRO — UTAH MEDICAL PRODUCTS, INC.MGC Diagnostics — MEDICAL GRAPHICS CORPORATIONVyaire — Jaeger Medical GmbHInnocor — Innovision ApS

Recent recalls

DateFirmReason
2024-10-11Baxter Healthcare CorporationThere is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.