DeviceClearance

TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001— 510(k) K000416

Substantially Equivalent

Retinalabs.Com

FDA 510(k) clearance K000416 for TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001, Substantially Equivalent on 2000-05-08. Applicant: Retinalabs.Com.

Clearance details

Applicant
Retinalabs.Com
Product code
Code MPA
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Atlanta, GA, US
Download summary PDFView on FDA.gov ↗

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