CANDI-KIT TM— 510(k) K854672

Substantially Equivalent

Culture Kits, Inc.

FDA 510(k) clearance K854672 for CANDI-KIT TM, Substantially Equivalent on 1986-07-11. Applicant: Culture Kits, Inc.. Device class: 1.

Clearance details

Applicant: Culture Kits, Inc.
Product code: Code JSI
Device class: Class 1
Regulation: 21 CFR 866.2360
Advisory panel: Microbiology
Date received: 1985-11-21
Decision date: 1986-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwich, NY, US

Download summary PDF View on FDA.gov ↗

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