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510(k) K022503

UTERINE INJECTOR by Thomas Medical, Inc. — Product Code LKF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 25, 2002
Date Received
July 29, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cannula, Manipulator/Injector, Uterine
Device Class
Class II
Regulation Number
884.4530
Review Panel
OB
Submission Type

Other clearances by Thomas Medical, Inc.

  • K022593 — THOMAS MEDICAL ELECTRODES (November 1, 2002)

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