Baxter Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Baxter Diagnostics, Inc. - FDA 510(k) Cleared Devices
Baxter Diagnostics, Inc. is a diagnostic device manufacturer based in Miami, US. The company specialized in microbiology and chemistry diagnostic solutions.
Baxter Diagnostics received 72 FDA 510(k) clearances from 72 total submissions between 1988 and 1995. The company's regulatory focus centered on microbiology devices, particularly dried antimicrobial susceptibility testing panels and related diagnostic assays. This historical record reflects the company's core expertise in microbial identification and resistance testing.
The company is no longer active in FDA 510(k) submissions, with no clearances recorded since 1995. This profile serves as a historical regulatory record for reference purposes. Explore the complete device clearance history, product codes, and submission dates in the database.
FDA 510(k) Regulatory Record - Baxter Diagnostics, Inc.
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