Abbott Mfg., Inc.
Abbott Mfg., Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1998.
Top product codes for Abbott Mfg., Inc.
Recent clearances by Abbott Mfg., Inc.
- K981457 — ALBP
- K981232 — CA
- K981231 — CO2
- K965230 — ABBOTT LIFECARE STANDARD TUBING INFUSION PUMP
- K971293 — LIFESHIELD PRIMARY I.V. SET WITH BACKCHECK VALVE
- K953656 — ABBOTT IMX PROLACTIN(MODIFICATION)
- K953657 — ABBOTT AXSYM PROLACTIN(MODIFICATION)
- K944669 — FLEXIFLO QUANTUM ENTERAL PUMP
- K943691 — IMX FOLATE
- K943733 — FLEXIFLO SIX ENTERAL NUTRITION PUMP
- K941214 — LIFESHIELD EXTENSION SET
- K940289 — ABBOTT PRISM ANALYZER
- K935376 — AXSYM GENTAMICIN
- K902753 — IMX ULTRASENTITIVE HTSH
Data sourced from openFDA. This site is unofficial and independent of the FDA.