Product code CAL— Anesthesiology
AO FLEXIBLE LARYNGOSCOPE, #LS-7
- Classification name
- Laryngoscope, Non-Rigid
- Device class
- Class 1
- Regulation
- 21 CFR 868.5530
- Advisory panel
- Anesthesiology
- Total cleared
- 8
- First cleared
- Most recent
Market context for product code CAL
FDA has cleared devices under product code CAL between 1979 and 1995, filed by 5 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1995
- 1988
- 1985
- 1980
- 1979
Top applicants under product code CAL
Adverse events under product code CAL
product code CAL- Malfunction
- 885
- Total
- 885
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 →
Recent clearances under product code CAL
- K951194 — FI-10M
- K951195 — FI-10P
- K872895 — HAEMONETICS CELL SAVER MINI SAVER AUTO. BLOOD SYS.
- K852994 — REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11
- K850978 — OLYMPUS LF-1 INTUBATION SCOPE
- K802331 — AO FLEXIBLE LARYNGOSCOPE, #LS-7
- K801364 — AO STYLET LARYNGOSCOPE MODEL SLS
- K791634 — AO STYLET LARYNGOSCOPE, MODEL SLS-1
Data sourced from openFDA. This site is unofficial and independent of the FDA.