100 ML SNYDER HEMOVAC

Apparatus, Suction, Single Patient Use, Portable, Nonpowered

SNYDER LABORATORIES, INC.

The following data is part of a premarket notification filed by Snyder Laboratories, Inc. with the FDA for 100 Ml Snyder Hemovac.

Pre-market Notification Details

Device IDK800542
510k NumberK800542
Device Name:100 ML SNYDER HEMOVAC
ClassificationApparatus, Suction, Single Patient Use, Portable, Nonpowered
Applicant SNYDER LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeGCY  
CFR Regulation Number878.4680 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1980-03-10
Decision Date1980-04-02

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