SIROPORT— 510(k) K800172

Substantially Equivalent

Siemens Corp.

FDA 510(k) clearance K800172 for SIROPORT, Substantially Equivalent on 1980-02-05. Applicant: Siemens Corp.. Device class: 1.

Clearance details

Applicant: Siemens Corp.
Product code: Code KLC
Device class: Class 1
Regulation: 21 CFR 872.6250
Advisory panel: Dental
Date received: 1980-01-25
Decision date: 1980-02-05
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.