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510(k) K932265

Device
SYMBIOSIS DISPOS PULMON BIOPSY FORCEPS W/REUS HAND
Applicant
SYMBIOSIS CORP.
510(k) number
K932265
Product code
FCL  
Decision
Substantially Equivalent (SESE)
Decision date
1993-08-09
Date received
1993-04-20
Regulation
876.1075
Classification name
Forceps, Biopsy, Non-electric
Medical specialty
Gastroenterology/Urology
Review panel
Gastroenterology/Urology
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
KEVIN W SMITH
Address
8600 NW 41 St. Miami FL US 33166 33166

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FCL  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K032092OLYMPUS XCYF-TP3 CYSTOFIBERSCOPE/NEPHROFIBERSCOPEOlympus Optical Co., Ltd.2003-07-16
K973611SPECTRASCIENCE REUSABLE BIOPSY FORCEPSSpectrascience, Inc.1997-12-02
K971315AUXILIARY INSTRUMENTS FOR URSRichard Wolf Medical Instruments Corp.1997-09-15
K964120INJECTO FLUSHRobert J. Jynch, Jr.1996-12-30
K963517SPECTRA SCIENCE BIOPSY FORCEPSSpectrascience, Inc.1996-12-02
K955065OLYMPUS FB SERIES BIOPSY FORCEPSOlympus America, Inc.1996-01-24
K952863FORCEPS, BIOPSY, NON-ELECTRICAnnex Medical, Inc.1995-07-19
K952391DYNABITE UROLOGICAL FORCEPSPortlyn Corp.1995-06-01
K951048RITE-BITE BIOPSY FORCEPSMill-Rose Laboratory1995-03-15
K946360MODULAR BIOPSY FORCEPCox Medical Ent., Inc.1995-03-06
K950559DIENER RETRIEVAL DEVICESMill-Rose Laboratory1995-02-16
K946238SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPSSymbiosis Corp.1995-01-20
K944770LSVP INTERNATIONAL BIOPSY FORCEPSLsvp Intl., Inc.1994-10-13
K941816EMC FLEXIBLE BIOPSY FORCEPSEnterprise Medical Corp.1994-07-13
K941359GIP/MEDI-GLOBE BIOPSY FORCEPSMedi-Globe Corp.1994-07-12

Legacy Summary#

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FDA Review#

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