DeviceClearance

MONITOR, PATIENT, RESP. CARBON DIOXIDE— 510(k) K770713

Substantially Equivalent

Cavitron Corp.

FDA 510(k) clearance K770713 for MONITOR, PATIENT, RESP. CARBON DIOXIDE, Substantially Equivalent on 1977-04-27. Applicant: Cavitron Corp.. Device class: 2.

Clearance details

Applicant
Cavitron Corp.
Product code
Code CCK
Device class
Class 2
Regulation
21 CFR 868.1400
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code CCK

view all

More clearances from Cavitron Corp.

view all

Adverse events under product code CCK

product code CCK
Death
3
Malfunction
11,428
Total
11,431

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.