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FDA 510(k) Application Details - K991285
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K991285
Device Name
Powered Laser Surgical Instrument
Applicant
AESCULAP-MEDITEC NORTH AMERICA
2525 MCGAW AVE.
IRVINE, CA 92623-9791 US
Other 510(k) Applications for this Company
Contact
WILLIAM KELLEY
Other 510(k) Applications for this Contact
Regulation Number
878.4810
More FDA Info for this Regulation Number
Classification Product Code
GEX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/15/1999
Decision Date
07/12/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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