CATHETERS, GREENLINE SUCTION— 510(k) K790606

Name: FDA 510(k) clearance K790606
Creator: U.S. Food and Drug Administration
Published: 1979-04-23

Substantially Equivalent

Snyder Laboratories, Inc.

FDA 510(k) clearance K790606 for CATHETERS, GREENLINE SUCTION, Substantially Equivalent on 1979-04-23. Applicant: Snyder Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Snyder Laboratories, Inc.
Product code: Code BSY
Device class: Class 1
Regulation: 21 CFR 868.6810
Advisory panel: Anesthesiology
Date received: 1979-03-29
Decision date: 1979-04-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BSY

view all

K031997 — MALLINCKRODT DAR TY-CARE / TY-CARE EXEL CLOSED SUCTION SYSTEM2003-11-25
K992902 — AMBU HAND POWER SUCTION PUMP1999-10-25
K982945 — DUAL PURPOSE CLOSED CATHETER1998-09-22
K981910 — SUCTION CATHETER1998-08-24
K972258 — HI-CARE CLOSED SUCTION SYSTEM1997-12-29

More clearances from Snyder Laboratories, Inc.

view all

K843906 — SNYDER HEMOVAC WOUND DRAINAGE DEVICES1984-11-05
K821321 — SNYDER DEBRIBEMENT SYSTEM LDP-11982-08-06
K800861 — SNYDER HEMOVAC CHEST DRAINAGE SOLUTION1980-05-02
K800543 — SNYDER HYSTERECTOMY Y TUBE KIT1980-04-16
K800577 — SNYDER HEMOVAC TM VENTED WOUND KIT1980-04-16

Adverse events under product code BSY

product code BSY

Death: 3
Injury: 155
Malfunction: 959
Total: 1,117

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.