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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K843717
Device Name VIRATEK SMALL PARTICLE AEROSOL GENERAT
Applicant
Viratek, Inc.
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Viratek, Inc.
4221 Richmond Rd., NW
Walker,  MI  49534
Date Received09/21/1984
Decision Date 12/30/1985
Decision Substantially Equivalent (SESE)
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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