BLAKEMORE TUBE

Tubes, Gastrointestinal (and Accessories)

INMED CORP.

The following data is part of a premarket notification filed by Inmed Corp. with the FDA for Blakemore Tube.

Pre-market Notification Details

Device IDK841038
510k NumberK841038
Device Name:BLAKEMORE TUBE
ClassificationTubes, Gastrointestinal (and Accessories)
Applicant INMED CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeKNT  
CFR Regulation Number876.5980 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1984-03-12
Decision Date1984-04-13

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