DeviceClearance

MOBIL-AIR— 510(k) K870064

Substantially Equivalent

Roman Laboratories, Inc.

FDA 510(k) clearance K870064 for MOBIL-AIR, Substantially Equivalent on 1987-02-11. Applicant: Roman Laboratories, Inc.. Device class: 2.

Clearance details

Applicant
Roman Laboratories, Inc.
Product code
Code CAW
Device class
Class 2
Regulation
21 CFR 868.5440
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Aurora, CO, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code CAW

product code CAW
Death
204
Injury
573
Malfunction
1,400
Other
6
Total
2,183

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.