OPTICHAMBER— 510(k) K962822
Substantially EquivalentHealthscan Products, Inc.
FDA 510(k) clearance K962822 for OPTICHAMBER, Substantially Equivalent on 1996-10-17. Applicant: Healthscan Products, Inc..
Clearance details
- Applicant
- Healthscan Products, Inc.
- Product code
- Code CAF
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Cedar Grove, NJ, US
Adverse events under product code CAF
product code CAF- Death
- 22
- Injury
- 125
- Malfunction
- 613
- Other
- 11
- Total
- 771
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.