MERETEK BREATH TEST FOR H.PYLORI COLLECTION KIT— 510(k) K952220

Substantially Equivalent

Meretek Diagnostics, Inc.

FDA 510(k) clearance K952220 for MERETEK BREATH TEST FOR H.PYLORI COLLECTION KIT, Substantially Equivalent on 1996-09-17. Applicant: Meretek Diagnostics, Inc..

Clearance details

Applicant: Meretek Diagnostics, Inc.
Product code: Code LYR
Advisory panel: Microbiology
Date received: 1995-05-11
Decision date: 1996-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

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Adverse events under product code LYR

product code LYR

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.