510(k) Report

FDA applicant

Therapeutics 101, Inc (Dba Pressure Point, Inc.)

Austin, TX1 decision2011–20110 recalls

FDA records 1 decision for Therapeutics 101, Inc (Dba Pressure Point, Inc.) (Austin, TX) in 2011: 1 510(k) clearance. All are in product code MVV (Device, Acupressure). 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

How often FDA has decided Therapeutics 101, Inc (Dba Pressure Point, Inc.)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2011: 1
2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Therapeutics 101, Inc (Dba Pressure Point, Inc.) by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • MVVDevice, Acupressure1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K110563Pressure Right, Single-Use, Disposable, Pressure-Sensitive Emetic-Management Wrist StripTherapeutics 101, Inc (Dba Pressure Point, Inc.) · 20111cites it

What has FDA decided for it lately?

  • K110563Pressure Right, Single-Use, Disposable, Pressure-Sensitive Emetic-Management Wrist StripTherapeutics 101, Inc (Dba Pressure Point, Inc.) · 2011

The one decision as Therapeutics 101, Inc (Dba Pressure Point, Inc.) →