GAS/PRES MONIT ENDOT TUB CONN/ADOP W/ & W/O TUB— 510(k) K852632

Substantially Equivalent

Medicomp, Inc.

FDA 510(k) clearance K852632 for GAS/PRES MONIT ENDOT TUB CONN/ADOP W/ & W/O TUB, Substantially Equivalent on 1986-01-03. Applicant: Medicomp, Inc..

Clearance details

Applicant: Medicomp, Inc.
Product code: Code CAI
Advisory panel: Anesthesiology
Date received: 1985-06-20
Decision date: 1986-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anoka, MN, US

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Adverse events under product code CAI

product code CAI

Malfunction: 869
Other: 1
Total: 870

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.