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510(k) K040565

PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE by Physician Industries, Inc. — Product Code GXD

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 22, 2004
Date Received
March 3, 2004
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Generator, Lesion, Radiofrequency
Device Class
Class II
Regulation Number
882.4400
Review Panel
NE
Submission Type

Other clearances by Physician Industries, Inc.

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  • K960248 — GENERAL PROCEDURE KIT (April 12, 1996)
  • K954068 — GENERAL HYGIENE KIT (November 8, 1995)

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