Medical Device Manufacturer · US , Abbott Park , IL

Abbott Mfg., Inc. - FDA 510(k) Cleared Devices

14 submissions · 13 cleared · Since 1990

Total

Cleared

Denied

Abbott Mfg., Inc. has 13 FDA 510(k) cleared medical devices. Based in Abbott Park, US.

Historical record: 13 cleared submissions from 1990 to 1998. Primary specialty: Chemistry.

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

FDA 510(k) Regulatory Record - Abbott Mfg., Inc.

14 devices

1-14 of 14

ABBOTT LIFECARE STANDARD TUBING INFUSION PUMP

K965230 · FRN

General Hospital · 184d

Cleared Jun 27, 1997

LIFESHIELD PRIMARY I.V. SET WITH BACKCHECK VALVE

K971293 · FPA

General Hospital · 81d

Cleared Oct 03, 1995

ABBOTT IMX PROLACTIN(MODIFICATION)

K953656 · CFT

Chemistry · 77d

Cleared Sep 25, 1995

ABBOTT AXSYM PROLACTIN(MODIFICATION)

K953657 · CFT

Chemistry · 69d

Cleared Jul 24, 1995

FLEXIFLO QUANTUM ENTERAL PUMP

K944669 · FRN

General Hospital · 314d

FLEXIFLO SIX ENTERAL NUTRITION PUMP

K943733 · LZH

General Hospital · 132d

Cleared Oct 03, 1994

LIFESHIELD EXTENSION SET

K941214 · FPK

General Hospital · 207d

Cleared Jul 18, 1994

ABBOTT PRISM ANALYZER

IMX ULTRASENTITIVE HTSH

K902753 · JLW

Chemistry · 18d

Abbott Mfg., Inc. - FDA 510(k) Cleared Devices

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