510(k) Report

FDA applicant

Rtc Inc.-Memcath Technologies, LLC

West St. Paul, MN2 decisions2006–20060 recalls

FDA records 2 decisions for Rtc Inc.-Memcath Technologies, LLC (West St. Paul, MN) in 2006: 2 510(k) clearances. Most are in product codes EOB (Nasopharyngoscope (Flexible Or Rigid)) and FED (Endoscopic Access Overtube…). Its devices cite 14 predicates, 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, ear, nose and throat panel, where it files most

How often FDA has decided Rtc Inc.-Memcath Technologies, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rtc Inc.-Memcath Technologies, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rtc Inc.-Memcath Technologies, LLC 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?

  • EOBNasopharyngoscope (Flexible Or Rigid)1decision
  • FEDEndoscopic Access Overtube, Gastroenterology-Urology1decision

Whose devices does it build on?

Its devices cite 14 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K061663Endomedical Technologies Quik-Cover Flexible Endoscope Barrier Sheath for Otolaryngoscopes and BronchoscopesRtc Inc.-Memcath Technologies, LLC · 2006
  • K061324Emt Quik-Cover Flexible Endoscope Barrier Sheath, Series 1-7Rtc Inc.-Memcath Technologies, LLC · 2006

All 2 as Rtc Inc.-Memcath Technologies, LLC →