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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name cannula, ophthalmic
510(k) Number K934844
Device Name INTER TIP T
Applicant
MICROSURGICAL TECHNOLOGY, INC.
723-B 9TH AVE.
KIRKLAND,  WA  98033
Applicant Contact SUSAN P AYLESWORTH
Correspondent
MICROSURGICAL TECHNOLOGY, INC.
723-B 9TH AVE.
KIRKLAND,  WA  98033
Correspondent Contact SUSAN P AYLESWORTH
Regulation Number886.4350
Classification Product Code
HMX  
Date Received10/08/1993
Decision Date 04/19/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
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