BLOOD RESERVOIR— 510(k) K770546

Name: FDA 510(k) clearance K770546
Creator: U.S. Food and Drug Administration
Published: 1977-04-26

Substantially Equivalent

Delta Medical Industries

FDA 510(k) clearance K770546 for BLOOD RESERVOIR, Substantially Equivalent on 1977-04-26. Applicant: Delta Medical Industries. Device class: 2.

Clearance details

Applicant: Delta Medical Industries
Product code: Code DTN
Device class: Class 2
Regulation: 21 CFR 870.4400
Advisory panel: Cardiovascular
Date received: 1977-03-21
Decision date: 1977-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Delta Medical Industries

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Adverse events under product code DTN

product code DTN

Death: 3
Total: 3

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.