Medical Device Manufacturer · US , Mchenry , IL

Monoclonal Antibodies, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1982

Total

Cleared

Denied

Monoclonal Antibodies, Inc. has 14 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1982 to 1988.

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

Monoclonal Antibodies, 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 - Monoclonal Antibodies, Inc.

14 devices

1-12 of 14

Cleared Feb 16, 1988

RAMP HERPES SIMPLEX VIRUS (HSV) (CCT)

K874863 · GQN

Microbiology · 83d

Cleared Jul 27, 1987

OVUQUICK SELF-TEST (OVUQUICK

RAMP PROGESTURINE PDG ASSAY--48 TEST KIT

MODEL SERUM HCG ASSAY

K850730 · JHI

Chemistry · 39d

Cleared Mar 05, 1985

OVU STICK SELF-TEST -MODIFICATION

OVU STICK URINE HLH KIT

K840412 · CEP

Chemistry · 73d

Cleared Jan 09, 1984

PREGNASTICK URINE HCG KIT

Monoclonal Antibodies, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Monoclonal Antibodies, Inc.

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