FITNESS LOGGER— 510(k) K840020

Name: FDA 510(k) clearance K840020
Creator: U.S. Food and Drug Administration
Published: 1984-10-26

Unknown

Britt Corp., Inc.

FDA 510(k) clearance K840020 for FITNESS LOGGER, Unknown on 1984-10-26. Applicant: Britt Corp., Inc.. Device class: 2.

Clearance details

Applicant: Britt Corp., Inc.
Product code: Code DPS
Device class: Class 2
Regulation: 21 CFR 870.2340
Advisory panel: Cardiovascular
Date received: 1984-01-05
Decision date: 1984-10-26
Decision: Unknown
Clearance type: Traditional
Location: Chanhassen, MN, US

Download summary PDF View on FDA.gov ↗

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K860977 — MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION1986-10-16
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Adverse events under product code DPS

product code DPS

Death: 7
Total: 7

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.