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MODIFICATION TO: ABBOTT VASCULAR SUTURE ANASTOMOSIS DEVICE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450559901·

ID NOW COVID-19

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 23, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 17, 2021

IDNOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 5, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·August 20, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·August 20, 2021

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00193033533291·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304007073·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304007035·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304007080·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304007059·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00193033533307·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00193033533314·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304007097·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304007042·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00193033533321·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00193033533277·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304006984·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00193033533253·