DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX— 510(k) K092827

Name: FDA 510(k) clearance K092827
Creator: U.S. Food and Drug Administration
Published: 2010-01-08

Substantially Equivalent

Dimeda Instrumente GmbH

FDA 510(k) clearance K092827 for DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX, Substantially Equivalent on 2010-01-08. Applicant: Dimeda Instrumente GmbH. Device class: 2.

Clearance details

Applicant: Dimeda Instrumente GmbH
Product code: Code HDA
Device class: Class 2
Regulation: 21 CFR 884.4400
Advisory panel: Obstetrics/Gynecology
Date received: 2009-09-14
Decision date: 2010-01-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tuttlingen, DE

Download summary PDF View on FDA.gov ↗

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