RESPIRONICS SUCTIONEASY— 510(k) K882017

Name: FDA 510(k) clearance K882017
Creator: U.S. Food and Drug Administration
Published: 1988-07-14

Substantially Equivalent

Respironics, Inc.

FDA 510(k) clearance K882017 for RESPIRONICS SUCTIONEASY, Substantially Equivalent on 1988-07-14. Applicant: Respironics, Inc.. Device class: 1.

Clearance details

Applicant: Respironics, Inc.
Product code: Code BSY
Device class: Class 1
Regulation: 21 CFR 868.6810
Advisory panel: Anesthesiology
Date received: 1988-05-13
Decision date: 1988-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Murrysville, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BSY

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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

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K243394 — AF531 Oro-Nasal SE Face Mask2024-12-30
K231313 — Therapy Mask 3100 NC/SP2023-07-28
K210844 — DreamWear Silicone Pillows Mask2021-08-24
K210386 — Magneto Nasal Mask2021-07-12
K202142 — Sleepware G32020-10-29

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.