SURGICAL LIGHT 22 SERIES— 510(k) K781581
Substantially EquivalentAmerican Sterilizer Co.
FDA 510(k) clearance K781581 for SURGICAL LIGHT 22 SERIES, Substantially Equivalent on 1978-10-17. Applicant: American Sterilizer Co..
Clearance details
- Applicant
- American Sterilizer Co.
- Product code
- Code FQP
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.