Medical Device Manufacturer · CA , Toronto, Ontario

Scican - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1991

Recent clearances: K-SPRAY, MODEL 085-2715, QUANTIM 16 AUTOCLAVE, STATIM 5000 CASSETTE AUTOCLAVE

View 9 510(k) Devices ↓

Total

Cleared

Denied

Scican has 9 FDA 510(k) cleared medical devices. Based in Toronto, Ontario, CA.

Historical record: 9 cleared submissions from 1991 to 2006. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Scican Filter by specialty or product code using the sidebar.

Scican is one of 680 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Scican

9 devices

1-9 of 9

Cleared Oct 19, 2006

K-SPRAY, MODEL 085-2715

General Hospital · 128d

Cleared Jan 04, 1999

STATIM 5000 CASSETTE AUTOCLAVE

K983679 · FLE

General Hospital · 76d

Cleared Feb 04, 1997

TCB TEMPORARY CROWN AND BRIDGE MATERIAL

K964691 · EBG

Dental · 74d

Cleared Jan 13, 1997

STAT IM 5000 CASSETTE AUTOCLAVE

K962179 · FLE

General Hospital · 221d

Cleared Oct 02, 1996

STERIMASTER AUTOCLAVE

K944036 · FLE

General Hospital · 776d

Cleared Jan 11, 1995

POLYSIL (VINYL POLYSILOXAN IMPRESSION MATERIAL)

K945142 · ELW

Dental · 83d

Cleared Aug 04, 1992

STATIM CASSETT AUTOCLAVE, MODIFICATION

K915054 · FLE

General Hospital · 274d

Cleared May 03, 1991

STATIM CASSETTE AUTOCLAVE

K910241 · FLE

General Hospital · 101d

Scican - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Scican

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