Medical Device Manufacturer · US , Hebron , IL

Filtertek, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1989

Total

Cleared

Denied

Filtertek, Inc. has 10 FDA 510(k) cleared medical devices. Based in Hebron, US.

Historical record: 10 cleared submissions from 1989 to 1998. Primary specialty: Gastroenterology & Urology.

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

Filtertek, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Filtertek, Inc.

10 devices

1-10 of 10

Cleared Jun 18, 1998

NFC NEEDLEFREE Y-SITE, MODEL 69970

K981547 · FPA

General Hospital · 49d

Cleared Jun 18, 1998

NFC NEEDLEFREE CONNECTOR MODEL 69900

K981548 · FPA

General Hospital · 49d

Cleared Jan 15, 1992

PN 62290 0.22 MICRON MICRO INFUS I.V. EXTEN SET

K914792 · FPA

General Hospital · 84d

Cleared Nov 29, 1991

I.V. FILTER EXTENSION SET

K912848 · FPB

General Hospital · 154d

Cleared Aug 30, 1991

TRANSDUCER PROTECTOR

K912394 · FIB

Gastroenterology & Urology · 94d

Cleared Jun 06, 1991

I.V. EXTENDER SET

K911451 · FPB

General Hospital · 64d

Cleared Jan 04, 1991

TRANSDUCER PROTECTOR

K904912 · FIB

Gastroenterology & Urology · 65d

Cleared Jul 27, 1990

TRANSDUCER PROTECTOR

K901409 · FIB

Gastroenterology & Urology · 123d

Cleared Jun 01, 1990

FILTERTEK PN 60650 DIALYSIS TRANSDUCER PROTECTOR

K901996 · FIB

Gastroenterology & Urology · 30d

Cleared Nov 08, 1989

TRANSDUCER PROTECTOR

K895281 · FIB

Gastroenterology & Urology · 76d

Filtertek, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Filtertek, Inc.

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