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FDA 510(k) Application Details - K020882
Device Classification Name
Plug, Punctum
More FDA Info for this Device
510(K) Number
K020882
Device Name
Plug, Punctum
Applicant
SURGICAL SPECIALTIES CORP.
100 DENNIS DR.
READING, PA 19606 US
Other 510(k) Applications for this Company
Contact
ELIZABETH LAZARO
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LZU
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/18/2002
Decision Date
07/26/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
OP - Ophthalmic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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