510(k) K850726

Device
WIRE CUTTERS, BRACHYTHERAPY-TABLE TOP & HAND HELD
Applicant
SYNCOR INTL. CORP.
510(k) number
K850726
Product code
IWA  
Decision
Substantially Equivalent (SESE)
Decision date
1985-03-26
Date received
1985-02-22
Regulation
892.5730
Classification name
Source, Wire, Iridium, Radioactive
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
ELEANOR V CHIU
Address
12847 Arroyo St. Sylmar CA US 91342 91342

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code IWA  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K915253IR-192 IMPLANT, MODIFICATIONOmnitron Intl., Inc.1992-02-27
K894409CESIUM-137 MICROSEED SOURCE TRAIN ASSEMBLY/SHIELDAmersham Corp.1989-09-29
K874895IR-192 IMPLANTRads S.L., Inc.1988-02-25
K850382IRIDIUM SEEDSRadiation Safety & Nuclear Products, Inc.1985-08-15
K844248IR-192 IMPLANTRads S.L., Inc.1985-04-10
K850163IRIDIUM 192 WIRESSyncor Intl. Corp.1985-03-26
K771878IRIDIUM 192 WIRES & PINSCis Radiopharmaceuticals, Inc.1977-10-27

Legacy Summary#

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FDA Review#

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