AIA-PACK PAP CALIBRATION VERIFICATION TEST SET— 510(k) K924854

Name: FDA 510(k) clearance K924854
Creator: U.S. Food and Drug Administration
Published: 1992-11-16

Substantially Equivalent

Tosoh Medics, Inc.

FDA 510(k) clearance K924854 for AIA-PACK PAP CALIBRATION VERIFICATION TEST SET, Substantially Equivalent on 1992-11-16. Applicant: Tosoh Medics, Inc.. Device class: 1.

Clearance details

Applicant: Tosoh Medics, Inc.
Product code: Code JJX
Device class: Class 1
Regulation: 21 CFR 862.1660
Advisory panel: Clinical Chemistry
Date received: 1992-09-28
Decision date: 1992-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code JJX

product code JJX

Other: 2
Total: 2

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.