ASPIRATION NEEDLE

Drape, Surgical

FERRIS MFG. CORP.

The following data is part of a premarket notification filed by Ferris Mfg. Corp. with the FDA for Aspiration Needle.

Pre-market Notification Details

Device IDK780784
510k NumberK780784
Device Name:ASPIRATION NEEDLE
ClassificationDrape, Surgical
Applicant FERRIS MFG. CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeKKX  
CFR Regulation Number878.4370 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1978-05-12
Decision Date1978-08-14

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