OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)— 510(k) K964445

Name: FDA 510(k) clearance K964445
Creator: U.S. Food and Drug Administration
Published: 1997-01-30

Substantially Equivalent

Dlp, Inc.

FDA 510(k) clearance K964445 for OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006), Substantially Equivalent on 1997-01-30. Applicant: Dlp, Inc.. Device class: 1.

Clearance details

Applicant: Dlp, Inc.
Product code: Code DWS
Device class: Class 1
Regulation: 21 CFR 870.4500
Advisory panel: Cardiovascular
Date received: 1996-11-06
Decision date: 1997-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Rapids, MI, 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.