Medical Device Manufacturer · US , Mchenry , IL

Quality Assurance Laboratory, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1980

Total

Cleared

Denied

Quality Assurance Laboratory, Inc. has 11 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.

Historical record: 11 cleared submissions from 1980 to 1980.

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

Quality Assurance Laboratory, 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 - Quality Assurance Laboratory, Inc.

11 devices

1-11 of 11

Cleared Jun 02, 1980

TRYPTICASE SOY AGAR W5% SHEEP BLOOD

XYLOSE LYSINE DESOXYCHOLATE AGAR

K800978 · JSH

Microbiology · 35d

Cleared May 28, 1980

CHOCOLATE AGAR W/ENRICHMENTS

MUELLER HINTIN AGAR W/5% SHEEP BLOOD

SALMONELLA SHIGELLA AGAR

EOSIN METHYLENE BLUE AGAR, LEVINE

K800984 · JSH

Microbiology · 30d

Cleared May 23, 1980

THIOGLYCOLLATE MED. W/O INDICATOR

K800985 · JSG

Microbiology · 30d

Quality Assurance Laboratory, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Quality Assurance Laboratory, Inc.

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