510(k) Report

Devices descending from K942677

6 later devices reach Geenen/Zebra Guidelines through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K011759Radius Next Generation GuidewireRadius Medical Technologies, Inc.20014—
+1K964780Bard Director Guidewire (000560)C.R. Bard, Inc.19970—
+2K050304FX Wire Advanced Measurement GuidewireConmedcorp20050—
+2K023603Endo-Glide GuidewireEndo-Therapeutics, Inc.20032—
+3K051068Zutron Colonoscope Stiffening DeviceZutron Medical20051—
+4K251204FUJIFILM Stiffening Wire Device (SW-2000)FUJIFILM Healthcare Americas Corporation20250—