FDA applicant

Akron City Hospital

Akron, OH2 decisions1984–19850 recalls

FDA records 2 decisions for Akron City Hospital (Akron, OH) from 1984 to 1985: 2 510(k) clearances. Most are in product codes FFT (Electrode, Ph, Stomach) and FFI (System, Alarm, Electrosurgical). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Akron City Hospital’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Akron City Hospital since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Akron”

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

Akron Catheter, Inc. 3 Akron Medical Corp. 1

Akron City Hospital

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Akron”