MODELS 246 AND 210F LINEAR ARRAY ULTRASOUND SCANNER— 510(k) K837304
Substantially EquivalentAloka Co., Ltd.
FDA 510(k) clearance K837304 for MODELS 246 AND 210F LINEAR ARRAY ULTRASOUND SCANNER, Substantially Equivalent on 1983-05-09. Applicant: Aloka Co., Ltd..
Clearance details
- Applicant
- Aloka Co., Ltd.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tokyo, JP
Data sourced from openFDA. This site is unofficial and independent of the FDA.