FDA applicant

Vitalog Corp.

Redwood, CA4 decisions1981–19880 recalls

FDA records 4 decisions for Vitalog Corp. (Redwood, CA) from 1981 to 1988: 4 510(k) clearances. Most are in product codes DPZ (Oximeter, Ear) and BZQ (Monitor, Breathing Frequency). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Vitalog Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vitalog Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vitalog Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vitalog Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Vitalog”

FDA records each applicant name separately; these may or may not be the same firm.

Vitalog Monitoring,Inc. 4

Vitalog Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Vitalog”