Medical Device Manufacturer · US , Mchenry , IL

Streck Laboratories, Inc. - FDA 510(k) Cleared Devices

70 submissions · 70 cleared · Since 1977

Total

Cleared

Denied

Streck Laboratories, Inc. has 70 FDA 510(k) cleared hematology devices. Based in Mchenry, US.

Historical record: 70 cleared submissions from 1977 to 2004.

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

Streck Laboratories, 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 - Streck Laboratories, Inc.

70 devices

1-12 of 70

Cleared Oct 19, 2004

RETIC-CHEX FOR CELL-DYN

SICKLE-CHEX SOLUBILITY KIT

K023656 · GHM

Hematology · 61d

Cleared Jun 25, 2002

MODIFICATION TO PARA 5X

Looking for a specific device from Streck Laboratories, Inc.? Search by device name or K-number.

Search all Streck Laboratories, Inc. devices

Streck Laboratories, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Streck Laboratories, Inc.

Filters