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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Instrument, Surgical, Non-Powered
510(k) Number K902850
Device Name ZEPPELIN INSTRUMENTS
Applicant
Ruggles Corp.
38 Billings Rd.
No. Quincy,  MA  02171
Applicant Contact ALAN RUGGLES
Correspondent
Ruggles Corp.
38 Billings Rd.
No. Quincy,  MA  02171
Correspondent Contact ALAN RUGGLES
Regulation Number882.4535
Classification Product Code
HAO  
Date Received06/29/1990
Decision Date 07/18/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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