FDA applicant

Viva-Tek Assoc., Inc.

Medford, NJ2 decisions1993–19940 recalls

FDA records 2 decisions for Viva-Tek Assoc., Inc. (Medford, NJ) from 1993 to 1994: 2 510(k) clearances. Most are in product codes CBN (Apparatus, Gas-Scavenging) and FRR (Chamber, Reverse Isolation, Patient Care). 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 Viva-Tek Assoc., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Viva-Tek Assoc., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Viva-Tek Assoc., Inc.

Which product codes does it file in?

What has FDA decided for it lately?