BIOTIS MOTILITY TEST MEDIUM— 510(k) K862392

Substantially Equivalent

Otisville Biotech, Inc.

FDA 510(k) clearance K862392 for BIOTIS MOTILITY TEST MEDIUM, Substantially Equivalent on 1986-07-03. Applicant: Otisville Biotech, Inc..

Clearance details

Applicant: Otisville Biotech, Inc.
Product code: Code JSF
Advisory panel: Microbiology
Date received: 1986-06-24
Decision date: 1986-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Otisville, NY, US

Download summary PDF View on FDA.gov ↗

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