MODEL 130 AUTOMATIC HEIGHT ADJUST (AHA) INCUBATOR— 510(k) K900735

Substantially Equivalent

Preemicare Corp.

FDA 510(k) clearance K900735 for MODEL 130 AUTOMATIC HEIGHT ADJUST (AHA) INCUBATOR, Substantially Equivalent on 1990-05-02. Applicant: Preemicare Corp..

Clearance details

Applicant: Preemicare Corp.
Product code: Code FMZ
Advisory panel: General Hospital
Date received: 1990-02-16
Decision date: 1990-05-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

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Adverse events under product code FMZ

product code FMZ

Death: 2
Malfunction: 457
Other: 1
Total: 460

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.