NEEDLE TECHNOLOGIES SEED IMPLANT NEEDLE— 510(k) K921886

Name: FDA 510(k) clearance K921886
Creator: U.S. Food and Drug Administration
Published: 1992-10-05

Substantially Equivalent

Needle Technologies, Inc.

FDA 510(k) clearance K921886 for NEEDLE TECHNOLOGIES SEED IMPLANT NEEDLE, Substantially Equivalent on 1992-10-05. Applicant: Needle Technologies, Inc.. Device class: 1.

Clearance details

Applicant: Needle Technologies, Inc.
Product code: Code IWJ
Device class: Class 1
Regulation: 21 CFR 892.5650
Advisory panel: Radiology
Date received: 1992-04-21
Decision date: 1992-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palm Harbor, FL, US

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