PHILLY INFANT BOLT— 510(k) K820151

Name: FDA 510(k) clearance K820151
Creator: U.S. Food and Drug Administration
Published: 1982-01-28

Substantially Equivalent

Philadelphia Medical Specialties

FDA 510(k) clearance K820151 for PHILLY INFANT BOLT, Substantially Equivalent on 1982-01-28. 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: 1982-01-19
Decision date: 1982-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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