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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name phosphomolybdate (colorimetric), inorganic phosphorus
510(k) Number K802159
Device Name AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS
Applicant
PANMED, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
PANMED, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number862.1580
Classification Product Code
CEO  
Date Received09/08/1980
Decision Date 10/10/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
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