FASTUBE NERVE REGENERATION DEVICE— 510(k) K850785

Name: FDA 510(k) clearance K850785
Creator: U.S. Food and Drug Administration
Published: 1985-07-10

Substantially Equivalent

Research Medical, Inc.

FDA 510(k) clearance K850785 for FASTUBE NERVE REGENERATION DEVICE, Substantially Equivalent on 1985-07-10. Applicant: Research Medical, Inc.. Device class: 2.

Clearance details

Applicant: Research Medical, Inc.
Product code: Code JXI
Device class: Class 2
Regulation: 21 CFR 882.5275
Advisory panel: Neurology
Date received: 1985-02-26
Decision date: 1985-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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