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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K772055
Device Name PENTAX F.O.-IT OBSERVER SCOPE
Applicant
Pilling Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Pilling Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Date Received10/31/1977
Decision Date 11/15/1977
Decision Substantially Equivalent (SESE)
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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