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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K840096
Device Name SEBUTAPE
Applicant
Cuderm Corp.
4221 Richmond Rd., NW
Walker,  MI  49534
Correspondent
Cuderm Corp.
4221 Richmond Rd., NW
Walker,  MI  49534
Date Received01/10/1984
Decision Date 08/02/1984
Decision Substantially Equivalent (SESE)
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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