Medical Device Manufacturer · US , Mchenry , IL

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

8 submissions · 7 cleared · Since 1984

Total

Cleared

Denied

Lyphomed, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1984 to 1991. Primary specialty: General Hospital.

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

Lyphomed, 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 - Lyphomed, Inc.

8 devices

1-8 of 8

Cleared May 14, 1991

SPARK KIT(R), MODIFICATION

K910142 · FPA

General Hospital · 120d

Cleared Feb 18, 1987

SPARK-KIT(TM)

K864509

General Hospital · 96d

Cleared Nov 12, 1985

NITROGLYCERIN INFUSION SET

K853019 · FPA

General Hospital · 118d

Cleared Aug 19, 1985

SECONDARY ADMINISTRATION SET

K853086 · FPA

General Hospital · 27d

Cleared Aug 16, 1985

VENTED SECONDARY IV ADMINISTRATION SET

K852881 · FPA

General Hospital · 38d

Cleared Aug 16, 1985

MAXIFILL TRANSFER SET

K852882 · LHI

General Hospital · 38d

Cleared Oct 09, 1984

I.V. TRANSFER SPIKE

K842678 · FPA

General Hospital · 91d

Cleared Aug 17, 1984

MAXIFILL TRANSFER SET

K842345 · LHI

General Hospital · 64d

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: Apr 27, 2026

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

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

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