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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name First Aid Kit With Drug
510(k) Number K841900
Device Name FIRST RESPONSE EMERG. EYE INJURIES
Applicant
Reed Products, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Reed Products, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Classification Product Code
LRR  
Date Received05/07/1984
Decision Date 07/23/1984
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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