ANTEC AIRWAY SAMPLING DEVICE W/MOISTURE TRAP— 510(k) K893919
Substantially EquivalentBaxter Healthcare Corp
FDA 510(k) clearance K893919 for ANTEC AIRWAY SAMPLING DEVICE W/MOISTURE TRAP, Substantially Equivalent on 1989-09-15. Applicant: Baxter Healthcare Corp. Device class: 1.
Clearance details
- Applicant
- Baxter Healthcare Corp
- Product code
- Code CAI
- Device class
- Class 1
- Regulation
- 21 CFR 868.5240
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Valencia, CA, US
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Adverse events under product code CAI
product code CAI- Malfunction
- 869
- Other
- 1
- Total
- 870
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.