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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K833884
Device Name ISOTEC DISPOS. PRESSURE TRANSDUCER
Applicant
Delta Medical Industries
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Delta Medical Industries
4221 Richmond Rd., NW
Walker,  MI  49534
Date Received11/09/1983
Decision Date 04/17/1984
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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