REMOVAWELL PLATE LID

Device, General Purpose, Microbiology, Diagnostic

DYNATECH CORP.

The following data is part of a premarket notification filed by Dynatech Corp. with the FDA for Removawell Plate Lid.

Pre-market Notification Details

Device IDK823557
510k NumberK823557
Device Name:REMOVAWELL PLATE LID
ClassificationDevice, General Purpose, Microbiology, Diagnostic
Applicant DYNATECH CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeLIB  
CFR Regulation Number866.2660 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-12-02
Decision Date1982-12-28

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