RATESAVER PLUS— 510(k) K952671

Name: FDA 510(k) clearance K952671
Creator: U.S. Food and Drug Administration
Published: 1995-08-18

Substantially Equivalent - Subject to Tracking Reg.

Entracare Corp.

FDA 510(k) clearance K952671 for RATESAVER PLUS, Substantially Equivalent - Subject to Tracking Reg. on 1995-08-18. Applicant: Entracare Corp.. Device class: 2.

Clearance details

Applicant: Entracare Corp.
Product code: Code LZH
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1995-06-12
Decision date: 1995-08-18
Decision: Substantially Equivalent - Subject to Tracking Reg.
Clearance type: Traditional
Location: Lenexa, KS, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LZH

product code LZH

Death: 12
Malfunction: 4,186
Total: 4,198

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.