Medical Device Manufacturer · US , Mchenry , IL

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

13 submissions · 13 cleared · Since 1981

Total

Cleared

Denied

Avi, Inc. has 13 FDA 510(k) cleared general hospital devices. Based in Mchenry, US.

Historical record: 13 cleared submissions from 1981 to 1988.

Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.

Avi, 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 - Avi, Inc.

13 devices

1-12 of 13

Cleared Aug 11, 1988

ENTRUST(TM) MODEL 800

K882047 · FRN

General Hospital · 87d

Cleared Apr 29, 1988

MODEL 210A INFUSION PUMP

K875347 · FRN

General Hospital · 120d

Cleared Apr 29, 1988

MODEL 400A INFUSION PUMP

K875348 · FRN

General Hospital · 120d

Cleared Apr 29, 1988

MODEL 200A INFUSION PUMP

K875365 · FRN

General Hospital · 120d

Cleared Dec 16, 1987

INFUSION PUMP MODEL 270

K872514 · FRN

General Hospital · 175d

Cleared Dec 16, 1987

INFUSION PUMP MODEL 470

K872515 · FRN

General Hospital · 175d

Cleared Dec 16, 1987

INFUSION PUMP MODEL 275

K872516 · FRN

General Hospital · 175d

Cleared Dec 10, 1985

MODEL 210 INFUSION PUMP

K854073 · FRN

General Hospital · 67d

Cleared Dec 10, 1985

MODEL 200 INFUSION PUMP

K854074 · FRN

General Hospital · 67d

Cleared Oct 31, 1984

AVI GUARDIAN MICRO 410 INFUSION PUMP

K843615 · FRN

General Hospital · 47d

Cleared Oct 31, 1984

AVI GUARDIAN 400 INFUSION PUMP

K843616 · FRN

General Hospital · 47d

Cleared Dec 22, 1982

GUARDIAN 110, VOL. CONTROL DELIV. SYS

K823406 · FRN

General Hospital · 37d

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

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

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