INDISCAL DIGITAL MANOMETER— 510(k) K102192

Substantially Equivalent

Baylis Medical Co., Inc.

FDA 510(k) clearance K102192 for INDISCAL DIGITAL MANOMETER, Substantially Equivalent on 2011-02-23. Applicant: Baylis Medical Co., Inc..

Clearance details

Applicant: Baylis Medical Co., Inc.
Product code: Code FMF
Advisory panel: General Hospital
Date received: 2010-08-04
Decision date: 2011-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mississauga, Ontario, CA

Download summary PDF View on FDA.gov ↗

Adverse events under product code FMF

product code FMF

Death: 15
Injury: 2,263
Malfunction: 29,722
Other: 17
Total: 32,017

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.