FDA Device Intelligence
Home › SALTER LABS › n/a

n/a

SALTER LABS · Model 6400 · UDI-DI 00607411007583

BZG Prescription
1
510(k) clearances
31
Adverse events
1
Recalls
94
Facilities

Description

DISPOSABLE SPIROMETER 10 Liter Calibrated Collection Bag DISPOSABLE (single patient use)

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 Communication System

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.