REUSABLE MLYOCARDIAL BIOPSY FORCEPS (BIOPTOMES— 510(k) K890453

Name: FDA 510(k) clearance K890453
Creator: U.S. Food and Drug Administration
Published: 1989-03-31

Substantially Equivalent

Dlp, Inc.

FDA 510(k) clearance K890453 for REUSABLE MLYOCARDIAL BIOPSY FORCEPS (BIOPTOMES, Substantially Equivalent on 1989-03-31. Applicant: Dlp, Inc.. Device class: 2.

Clearance details

Applicant: Dlp, Inc.
Product code: Code DWZ
Device class: Class 2
Regulation: 21 CFR 870.4075
Advisory panel: Cardiovascular
Date received: 1989-01-30
Decision date: 1989-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Rapids, MI, US

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