STOPCOCK— 510(k) K780596

Name: FDA 510(k) clearance K780596
Creator: U.S. Food and Drug Administration
Published: 1978-04-19

Substantially Equivalent

Abco Dealers, Inc.

FDA 510(k) clearance K780596 for STOPCOCK, Substantially Equivalent on 1978-04-19. Applicant: Abco Dealers, Inc.. Device class: 2.

Clearance details

Applicant: Abco Dealers, Inc.
Product code: Code FMG
Device class: Class 2
Regulation: 21 CFR 880.5440
Advisory panel: General Hospital
Date received: 1978-04-10
Decision date: 1978-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K210516 — Clicky Cross2022-05-16

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K880894 — ALLERGIST SYRINGES1988-03-31
K872875 — STRETCH GAUZE BANDAGES1987-09-04

Adverse events under product code FMG

product code FMG

Death: 14
Malfunction: 3,433
Other: 1
Total: 3,448

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.