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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Instrument, Manual, Surgical, General Use
510(k) Number K930775
Device Name DISPOSABLE FORCEPS, HEMOSTATS, NEEDLE GUIDES, ETC
Applicant
Falcon Instruments, Inc.
P.O. Box 3738
Arlington,  VA  22203
Applicant Contact ISMAIL
Correspondent
Falcon Instruments, Inc.
P.O. Box 3738
Arlington,  VA  22203
Correspondent Contact ISMAIL
Regulation Number878.4800
Classification Product Code
MDM  
Date Received02/16/1993
Decision Date 04/23/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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