PEDIATRIC VISION SCANNER— 510(k) DEN130051

Unknown

Rebiscan, Inc.

FDA 510(k) clearance DEN130051 for PEDIATRIC VISION SCANNER, Unknown on 2016-06-08. Applicant: Rebiscan, Inc.. Device class: 2.

Clearance details

Applicant
Rebiscan, Inc.
Product code
Code PMW
Device class
Class 2
Regulation
21 CFR 886.1342
Advisory panel
Ophthalmic
Date received
Decision date
Decision
Unknown
Clearance type
Direct
Location
Cambridge, MA, US
View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.