FDA 510(k) Application Details - K021831

Device Classification Name	Plug, Punctum   More FDA Info for this Device
510(K) Number	K021831
Device Name	Plug, Punctum
Applicant	LACRIMEDICS, INC. 310 PRUNE ALLEY EASTSOUND, WA 98245 US Other 510(k) Applications for this Company
Contact	JERRY HENDERSON 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	06/04/2002
Decision Date	07/01/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review