510(k) Report

FDA applicant

Mega Medical, Inc.

Tampa, FL7 decisions1991–19920 recalls

FDA records 7 decisions for Mega Medical, Inc. (Tampa, FL) from 1991 to 1992: 7 510(k) clearances. Most are in product codes CAZ (Anesthesia Conduction Kit) and DQY (Catheter, Percutaneous). 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 Mega Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mega Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Mega”

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