MYOCARD BIOPSY FORCEP— 510(k) K881412

Name: FDA 510(k) clearance K881412
Creator: U.S. Food and Drug Administration
Published: 1988-09-08

Substantially Equivalent

Fehling Medizintechnik GmbH

FDA 510(k) clearance K881412 for MYOCARD BIOPSY FORCEP, Substantially Equivalent on 1988-09-08. Applicant: Fehling Medizintechnik GmbH. Device class: 2.

Clearance details

Applicant: Fehling Medizintechnik GmbH
Product code: Code DWZ
Device class: Class 2
Regulation: 21 CFR 870.4075
Advisory panel: Cardiovascular
Date received: 1988-04-04
Decision date: 1988-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Germany, DE

Download summary PDF View on FDA.gov ↗

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