RABEA DEVICE, MODEL PXXXXXX— 510(k) K990345

Unknown

Signus Medizintechnik GmbH

FDA 510(k) clearance K990345 for RABEA DEVICE, MODEL PXXXXXX, Unknown on 1999-07-30. Applicant: Signus Medizintechnik GmbH. Device class: 2.

Clearance details

Applicant: Signus Medizintechnik GmbH
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1999-02-04
Decision date: 1999-07-30
Decision: Unknown
Clearance type: Traditional
Location: Shorewood, MN, 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.