DeviceClearance

MK 808 SERIES NASAL OXYGEN SAMPLER— 510(k) K822608

Substantially Equivalent

Instrumentation Industries, Inc.

FDA 510(k) clearance K822608 for MK 808 SERIES NASAL OXYGEN SAMPLER, Substantially Equivalent on 1982-10-04. Applicant: Instrumentation Industries, Inc.. Device class: 2.

Clearance details

Applicant
Instrumentation Industries, Inc.
Product code
Code CCL
Device class
Class 2
Regulation
21 CFR 868.1720
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code CCL

product code CCL
Other
2
Total
2

Source: openFDA MAUDE database, through . 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.