510(k) Report

FDA applicant

Condor Medical

No Salt Lake City, UT3 decisions1987–19880 recalls

FDA records 3 decisions for Condor Medical (No Salt Lake City, UT) from 1987 to 1988: 3 510(k) clearances. Most are in product codes DQX (Wire, Guide, Catheter) and JAA (System, X-Ray, Fluoroscopic, Image-Intensified). 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 Condor Medical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Condor Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Condor Medical 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?

  • DQXWire, Guide, Catheter1decision
  • JAASystem, X-Ray, Fluoroscopic, Image-Intensified1decision
  • FMFSyringe, Piston1decision

What has FDA decided for it lately?

  • K873985Fluoro CoverCondor Medical · 1988
  • K873942Guide Wire BowlCondor Medical · 1987
  • K8737093 Ring Attachment for SyringesCondor Medical · 1987

All 3 as Condor Medical →

Other applicant names beginning “Condor”

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

Condor Instruments Ltda. - Epp 1Condor Products, Inc. 1