Boston Scientific Corp
Boston Scientific Corp holds FDA 510(k) medical device clearances, first cleared 1988, most recent 2024, with 7 FDA device recalls on record.
Clearances by Boston Scientific Corp — page 5
401–432 of 432- K900205 — DRAINAGE CATHETERS W/A DISSOLVABLE TIP
- K910995 — MEDI-TECH BALLOON DILATATION CATHETER
- K911203 — TEGWIRE (TM)
- K910931 — BILIARY BALLOON DILATATION CATHETER
- K896520 — OWENS CATHETER
- K904788 — MEWISSEN CATHETER
- K904394 — INFLATION/DEFLATION DEVICE
- K901659 — TITANIUM GREENFIELD(R) VENA CAVA FILTER W/HOOKS
- K903813 — URETERAL BALLOON DILATATION CATHETER
- K900094 — PE-MT 5 MEDI-TECH BALLOON DILATATION CATHETER
- K897106 — MEDI-TECH DILATATION CATHETERS ULTRA THIN II
- K901235 — GREENFIELD VENA CAVA FILTER W/19.5 FR INTRODUCER
- K902245 — SONICATH(TM) 9F, 12 MHZ
- K902370 — MODIFIED PROSTATIC URETHROPLASTY BALLOON CATHETER
- K902124 — DOWD CATHETER
- K897124 — SMALL VESSEL BALLOON DILATATION CATHETER
- K901018 — MODIFIED TRANSLUMINAL BALLOON DILATATION CATHETERS
- K900281 — SERIES 3001 IABP
- K895542 — SONICATH(TM) 5 F
- K896920 — SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATHETER
- K897152 — CRAGG CONVERTIBLE WIRE
- K896597 — THE SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATH.
- K891121 — MEDI-TECH AMPLATZ INTRODUCER SHEALTH SYSTEM
- K894942 — SIDEWINDER 40CC DL INTRA-AORTIC BALLOON CATHETER
- K885168 — RUBENSTEIN URETERAL STONE FRAGMENT BRUSH
- K891580 — INTRAVASCULAR CATHETER WITH HYDROPHILIC COATING
- K892648 — MICROVASIVE ENDOTORQUE GUIDEWIRE, CAT #5177
- K891968 — ESP RADIATION REDUCTION EXAMINATION GLOVES
- K890772 — ULTRASONIC IMAGING CATHETER FOR CARDIAC APPLI.
- K885169 — STAMEY SAMPLER SPRING LOADED BIOPSY NEEDLE
- K885005 — MICROVASIVE GOLD PROBE
- K883202 — ULTRASONIC IMAGING CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.