FDA applicant

Procedure Packs, Inc.

Scottsdale, AZ4 decisions1988–19890 recalls

FDA records 4 decisions for Procedure Packs, Inc. (Scottsdale, AZ) from 1988 to 1989: 4 510(k) clearances. Most are in product codes DTL (Adaptor, Stopcock, Manifold, Fitting…) and DQD (Stethoscope, Electronic). 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, cardiovascular panel, where it files most

How often FDA has decided Procedure Packs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Procedure Packs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Procedure”

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

Procedure Products, Inc. 16 Procedure Pak, Inc. 2

Procedure Packs, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Procedure”