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FDA 510(k) Application Details - K992950
Device Classification Name
Lenses, Soft Contact, Daily Wear
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510(K) Number
K992950
Device Name
Lenses, Soft Contact, Daily Wear
Applicant
PROSTHETIC SOFT LENS CORP.
2890 SOUTH TEJON ST.
ENGLEWOOD, CO 80110 US
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Contact
WILLIAM HOFFMAN
Other 510(k) Applications for this Contact
Regulation Number
886.5925
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Classification Product Code
LPL
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More FDA Info for this Product Code
Date Received
09/01/1999
Decision Date
11/18/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OP - Ophthalmic
Review Advisory Committee
OP - Ophthalmic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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