SENSORMEDICS MICROGARD MICROBIAL FILTER— 510(k) K934272

Name: FDA 510(k) clearance K934272
Creator: U.S. Food and Drug Administration
Published: 1993-11-24

Substantially Equivalent

Sensor Medics Corp.

FDA 510(k) clearance K934272 for SENSORMEDICS MICROGARD MICROBIAL FILTER, Substantially Equivalent on 1993-11-24. Applicant: Sensor Medics Corp.. Device class: 2.

Clearance details

Applicant: Sensor Medics Corp.
Product code: Code CAH
Device class: Class 2
Regulation: 21 CFR 868.5260
Advisory panel: Anesthesiology
Date received: 1993-08-31
Decision date: 1993-11-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Yorba Linda, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CAH

view all

K252643 — Iso-Gard Filter Straight; Humid-Vent Filter Compact Angled2026-05-15
K251583 — Ambu® Virobac II® Exhalation Filter2026-04-30
K241339 — Besmed Bacterial Filter and HMEF2024-11-14
K222917 — Breathing circuit bacterial/viral filter2024-02-15
K230483 — Passy Muir Tracheostomy Viral & Bacterial Airway Protection Filter (PM-APF15)2023-09-16

More clearances from Sensor Medics Corp.

view all

K032516 — HIOX80 AEROSOL ADAPTER2004-03-04
K031745 — INFANT FLOW PLUS INFANT CPAP SYSTEM WITH SIPAP FUNCTION2004-02-13
K031883 — LYRA NASAL MASK2003-08-25
K030943 — MODIFICATION TO HIOX2003-04-22
K022192 — PEGASUS NASAL CPAP SYSTEM2003-01-24

Adverse events under product code CAH

product code CAH

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.