Home › Device types › BZG
Spirometer, Diagnostic
FDA product code BZG · Class 2 · Anesthesiology
1,170
Registered devices
31
Adverse events
1
Recalls
228
510(k) clearances
Devices with this code
PULMO-PROTECT™ LUNG FUNCTION FILTER, MOUTHPIECE AND NOSE CLIP — Intersurgical IncorporatedPolytech Filter — POLYTECHNIC RESOURCES INCPolytech Filter — POLYTECHNIC RESOURCES INCVyaire — Jaeger Medical GmbHCardio Q50, Cardio Q70 — Bionet CO,LTDVyaire — Jaeger Medical GmbHPolytech Filter — POLYTECHNIC RESOURCES INCPolytech Filter — POLYTECHNIC RESOURCES INCCuraplex — TRI-ANIM HEALTH SERVICES, INC.Filtrette with Mini Mouthpiece — S D I DIAGNOSTICS INCAstra Spirometer — S D I DIAGNOSTICS INCModel 4000 — VITALOGRAPH (IRELAND) LIMITEDAstra Spirometer — S D I DIAGNOSTICS INCMIR — MIR MEDICAL INTERNATIONAL RESEARCH SPAPFT — VITALOGRAPH (IRELAND) LIMITEDPFT — VITALOGRAPH (IRELAND) LIMITEDPolytech Filter — POLYTECHNIC RESOURCES INCModel 4000 — VITALOGRAPH (IRELAND) LIMITEDMedline — MEDLINE INDUSTRIES, INC.Astraguard — S D I DIAGNOSTICS INCAlpha — VITALOGRAPH (IRELAND) LIMITEDPolytech Filter — POLYTECHNIC RESOURCES INCAstra Spirometer — S D I DIAGNOSTICS INCModel 4000 — VITALOGRAPH (IRELAND) LIMITED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-10-11 | Baxter Healthcare Corporation | There 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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