SIEMENS INTRAVAGINAL TRANSDUCER— 510(k) K881405

Name: FDA 510(k) clearance K881405
Creator: U.S. Food and Drug Administration
Published: 1988-08-02

Substantially Equivalent

Siemens Medical Solutions USA, Inc.

FDA 510(k) clearance K881405 for SIEMENS INTRAVAGINAL TRANSDUCER, Substantially Equivalent on 1988-08-02. Applicant: Siemens Medical Solutions USA, Inc.. Device class: 2.

Clearance details

Applicant: Siemens Medical Solutions USA, Inc.
Product code: Code HGL
Device class: Class 2
Regulation: 21 CFR 884.2960
Advisory panel: Obstetrics/Gynecology
Date received: 1988-04-04
Decision date: 1988-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Iselin, NJ, US

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