Medical Device Manufacturer · US , Mchenry , IL

The Kendal Co. - FDA 510(k) Cleared Devices

63 submissions · 60 cleared · Since 1980

63

Total

60

Cleared

0

Denied

FDA 510(k) Regulatory Record - The Kendal Co. Cardiovascular ✕

7 devices

1-7 of 7

Cleared Jan 17, 1995

KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM

Cardiovascular · 225d

Cleared Oct 31, 1986

MODIFIED MODEL 5320 T.E.D. COMPRESSION LIMB

Cardiovascular · 46d

Cleared Jul 11, 1986

CURITY CENTRAL VENOUS CATHETERIZATION TRAY

Cardiovascular · 60d

Cleared Jul 10, 1986

CURITY VENOUS CATHETERIZATION KIT

Cardiovascular · 59d

Cleared Jul 10, 1986

CURITY CENTRAL VENOUS CATHETER

Cardiovascular · 59d

Cleared Apr 16, 1986

CURITY PERCUTANEOUS CATHETER INSERTION TRAY

Cardiovascular · 119d

Cleared Apr 16, 1986

CURITY PERCUTANEOUS CATHETER INSERTION KIT

Cardiovascular · 119d