TUBULAR STOCKINETTE

Bandage, Elastic

STAN-PAK ENT.

The following data is part of a premarket notification filed by Stan-pak Ent. with the FDA for Tubular Stockinette.

Pre-market Notification Details

Device IDK820142
510k NumberK820142
Device Name:TUBULAR STOCKINETTE
ClassificationBandage, Elastic
Applicant STAN-PAK ENT. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeFQM  
CFR Regulation Number880.5075 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-01-19
Decision Date1982-02-05

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