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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Counter, Cell, Automated (Particle Counter)
510(k) Number K952308
Device Name COULTER Z 1
Applicant
Coulter Corp.
11800 SW 147th Ave.
Mail Code 31-B06
Miami,  FL  33196
Applicant Contact BENITA BRADFORD-BOURQUE
Correspondent
Coulter Corp.
11800 SW 147th Ave.
Mail Code 31-B06
Miami,  FL  33196
Correspondent Contact BENITA BRADFORD-BOURQUE
Regulation Number864.5200
Classification Product Code
GKL  
Date Received05/17/1995
Decision Date 10/06/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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