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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K844757
Device Name TUBING HOLDER
Applicant
Procter & Gamble Mfg. Co.
P.O. Box 599
Cincinnati,  OH  45201
Applicant Contact JAMES T O'REILLY
Correspondent
Procter & Gamble Mfg. Co.
P.O. Box 599
Cincinnati,  OH  45201
Correspondent Contact JAMES T O'REILLY
Date Received12/07/1984
Decision Date 12/17/1984
Decision Substantially Equivalent (SESE)
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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