C-SPLINT— 510(k) K802104

Substantially Equivalent

Cutter Laboratories, Inc.

FDA 510(k) clearance K802104 for C-SPLINT, Substantially Equivalent on 1980-09-16. Applicant: Cutter Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Cutter Laboratories, Inc.
Product code: Code IQI
Device class: Class 1
Regulation: 21 CFR 890.3475
Advisory panel: Physical Medicine
Date received: 1980-09-03
Decision date: 1980-09-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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