FDA 510(k) Application Details - K001737

Device Classification Name	Plug, Punctum   More FDA Info for this Device
510(K) Number	K001737
Device Name	Plug, Punctum
Applicant	LACRIMEDICS, INC. 310 PRUNE ALLEY EASTSOUND, WA 98245 US Other 510(k) Applications for this Company
Contact	BRIAN P LOGAN 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	06/07/2000
Decision Date	06/19/2000
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