BIOPSY ATTACHMENT— 510(k) K831317

Substantially Equivalent

Diasonics, Inc.

FDA 510(k) clearance K831317 for BIOPSY ATTACHMENT, Substantially Equivalent on 1983-05-18. Applicant: Diasonics, Inc.. Device class: 2.

Clearance details

Applicant: Diasonics, Inc.
Product code: Code FCI
Device class: Class 2
Regulation: 21 CFR 876.1075
Advisory panel: Gastroenterology, Urology
Date received: 1983-04-22
Decision date: 1983-05-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.