MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES— 510(k) K952323

Name: FDA 510(k) clearance K952323
Creator: U.S. Food and Drug Administration
Published: 1995-06-23

Substantially Equivalent

Mist, Inc.

FDA 510(k) clearance K952323 for MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES, Substantially Equivalent on 1995-06-23. Applicant: Mist, Inc.. Device class: 2.

Clearance details

Applicant: Mist, Inc.
Product code: Code JOS
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1995-05-18
Decision date: 1995-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

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