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FDA 510(k) Application Details - K030906
Device Classification Name
Light, Surgical, Ceiling Mounted
More FDA Info for this Device
510(K) Number
K030906
Device Name
Light, Surgical, Ceiling Mounted
Applicant
ALM
1777 EAST HENRIETTA RD.
ROCHESTER, NY 14623 US
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Contact
FREDERICK R CATT
Other 510(k) Applications for this Contact
Regulation Number
878.4580
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Classification Product Code
FSY
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More FDA Info for this Product Code
Date Received
03/24/2003
Decision Date
04/23/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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