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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Forceps, Tube Introduction
510(k) Number K880319
Device Name MAGILL FORCEPS
Applicant
EASTMED ENTERPRISES INC.
5 PEMBURY COURT
MARLTON,  NJ  08053
Applicant Contact SUPTI PUTATUNDA
Correspondent
EASTMED ENTERPRISES INC.
5 PEMBURY COURT
MARLTON,  NJ  08053
Correspondent Contact SUPTI PUTATUNDA
Regulation Number868.5780
Classification Product Code
BWB  
Date Received01/26/1988
Decision Date 03/21/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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