FDA applicant

Pressure-Tech, Inc.

Great Neck, NY1 decision2010–20100 recalls

FDA records 1 decision for Pressure-Tech, Inc. (Great Neck, NY) in 2010: 1 510(k) clearance. All are in product code CBF (Chamber, Hyperbaric). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Pressure-Tech, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Pressure-Tech, Inc. by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Pressure-Tech, 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 “Pressure-Tech”

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

Pressure Products Medical Device Manufacturing, LLC 9 Pressure Point, Inc. 1 Pressure Products, Inc. 1

Pressure-Tech, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Pressure-Tech”