510(k) Report

FDA applicant

Polaroid Medical Corp.

Washington, DC1 decision1991–19910 recalls

FDA records 1 decision for Polaroid Medical Corp. (Washington, DC) in 1991: 1 510(k) clearance. All are in product code LMC (Camera, Multi Format, Radiological). 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, radiology panel, where it files most

How often FDA has decided Polaroid Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Polaroid Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • LMCCamera, Multi Format, Radiological1decision

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K912073Polaroid Helios Laser ImagerPolaroid Medical Corp. · 19912cite it

What has FDA decided for it lately?

  • K912073Polaroid Helios Laser ImagerPolaroid Medical Corp. · 1991

The one decision as Polaroid Medical Corp. →

Other applicant names beginning “Polaroid”

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

Polaroid Corp. 5