DELTA-LITE CASTING RESIN— 510(k) K854341

Name: FDA 510(k) clearance K854341
Creator: U.S. Food and Drug Administration
Published: 1985-11-22

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K854341 for DELTA-LITE CASTING RESIN, Substantially Equivalent on 1985-11-22. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 1.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code LGF
Device class: Class 1
Regulation: 21 CFR 888.5940
Advisory panel: Orthopedic
Date received: 1985-10-28
Decision date: 1985-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

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