OMNI-JUG— 510(k) K952200

Substantially Equivalent

Waterstone Medical, Inc.

FDA 510(k) clearance K952200 for OMNI-JUG, Substantially Equivalent on 1995-06-29. Applicant: Waterstone Medical, Inc.. Device class: 1.

Clearance details

Applicant: Waterstone Medical, Inc.
Product code: Code KDG
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1995-05-10
Decision date: 1995-06-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethesda, MD, 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.