MONITOR/MINI SCOPE— 510(k) K781679

Name: FDA 510(k) clearance K781679
Creator: U.S. Food and Drug Administration
Published: 1978-12-12

Substantially Equivalent

Ipco Corp.

FDA 510(k) clearance K781679 for MONITOR/MINI SCOPE, Substantially Equivalent on 1978-12-12. Applicant: Ipco Corp.. Device class: 2.

Clearance details

Applicant: Ipco Corp.
Product code: Code DPS
Device class: Class 2
Regulation: 21 CFR 870.2340
Advisory panel: Cardiovascular
Date received: 1978-10-02
Decision date: 1978-12-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K842836 — SAFE & SOFT MINI PADS & MAXI PADS1984-10-15
K842837 — SAFE & SOFT MAXI SHILEDS1984-10-15

Adverse events under product code DPS

product code DPS

Death: 7
Total: 7

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.