Home / 510(k) Clearances / K993735

510(k) K993735

DOUBLE SPRINGERS by Medtech Products , Ltd. — Product Code HIS

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 20, 2000
Date Received
November 4, 1999
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Condom
Device Class
Class II
Regulation Number
884.5300
Review Panel
OB
Submission Type

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