AMERIMED AS110— 510(k) K953069

Name: FDA 510(k) clearance K953069
Creator: U.S. Food and Drug Administration
Published: 1995-08-31

Substantially Equivalent

Amerimed Systems L.C.

FDA 510(k) clearance K953069 for AMERIMED AS110, Substantially Equivalent on 1995-08-31. Applicant: Amerimed Systems L.C.. Device class: 2.

Clearance details

Applicant: Amerimed Systems L.C.
Product code: Code FNM
Device class: Class 2
Regulation: 21 CFR 880.5550
Advisory panel: General Hospital
Date received: 1995-06-30
Decision date: 1995-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Desoto, TX, US

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K972022 — ZAK-20001998-01-22
K974319 — MIGHTY AIR1998-01-22
K974070 — PHYSIO/10001998-01-06
K972549 — SIMPULSE1997-11-18

Adverse events under product code FNM

product code FNM

Death: 22
Injury: 349
Other: 4
Total: 375

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.