510(k) Report

FDA applicant

Edward Manougian, M.D.

Berkeley, CA1 decision1984–19840 recalls

FDA records 1 decision for Edward Manougian, M.D. (Berkeley, CA) in 1984: 1 510(k) clearance. All are in product code BSY (Catheters, Suction, Tracheobronchial). 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, anesthesiology panel, where it files most

How often FDA has decided Edward Manougian, M.D.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Edward Manougian, M.D. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Edward”

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