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TECHNOLAS 217A EXCIMER LASER SYSTEM

FDA premarket approval P990027/S001 · decided 2000-12-22

Approval details

PMA number
P990027
Supplement
S001
Supplement type
Normal 180 Day Track
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
TECHNOLAS 217A EXCIMER LASER SYSTEM
Generic name
Excimer laser system
Applicant
Technolas Perfect Vision GmbH
Date received
2000-10-13
Decision date
2000-12-22
Days to decision
70 days
Decision code
APPR
Product code
LZS
Advisory committee
Ophthalmic
Expedited review
No
Location
München
Statement
APPROVAL FOR A MANUFACTURING SITE LOCATED AT TECHNOLAS GMBH, KIRCHEIM/HEIMSTETTEN, GERMANY.

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510(k) clearances by this applicant

RecordFirmDate
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VICTUS FEMTOSECOND LASER PLATFORM (K141379)Technolas Perfect Vision GmbH2015-01-16
VICTUS FEMTOSECOND LASER PLATFORM (K140615)Technolas Perfect Vision GmbH2014-07-15
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VICTUS FEMTOSECOND LASER PLATFORM (K122386)Technolas Perfect Vision GmbH2013-02-08
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