SYMBIOSIS BONE MARROW BIOPSY NEEDLE

Needle, Aspiration And Injection, Disposable

SYMBIOSIS CORP.

The following data is part of a premarket notification filed by Symbiosis Corp. with the FDA for Symbiosis Bone Marrow Biopsy Needle.

Pre-market Notification Details

Device IDK925416
510k NumberK925416
Device Name:SYMBIOSIS BONE MARROW BIOPSY NEEDLE
ClassificationNeedle, Aspiration And Injection, Disposable
Applicant SYMBIOSIS CORP. 8600 N.W. 41 ST. Miami,  FL  33166
ContactKevin W Smith
CorrespondentKevin W Smith
SYMBIOSIS CORP. 8600 N.W. 41 ST. Miami,  FL  33166
Product CodeGAA  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-10-27
Decision Date1993-02-23

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