PHILLY BOLT ADULT PROCEDURE KIT— 510(k) K823459

Name: FDA 510(k) clearance K823459
Creator: U.S. Food and Drug Administration
Published: 1982-12-22

Substantially Equivalent

Philadelphia Medical Specialties

FDA 510(k) clearance K823459 for PHILLY BOLT ADULT PROCEDURE KIT, Substantially Equivalent on 1982-12-22. Applicant: Philadelphia Medical Specialties. Device class: 2.

Clearance details

Applicant: Philadelphia Medical Specialties
Product code: Code GWN
Device class: Class 2
Regulation: 21 CFR 882.1460
Advisory panel: Neurology
Date received: 1982-11-18
Decision date: 1982-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.