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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K844073
Device Name SEERAM BLADE
Applicant
Seeram Products Development
465 20th Ave.
Vero Beach,  FL  32960
Applicant Contact RIBIN SEERAM
Correspondent
Seeram Products Development
465 20th Ave.
Vero Beach,  FL  32960
Correspondent Contact RIBIN SEERAM
Date Received10/19/1984
Decision Date 11/19/1984
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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