BLEASE FRONTLINE PLUS RANGE, ANESTHESIA MACHINES, MODEL 440, 560 AND 690— 510(k) K003251

Substantially Equivalent

Blease Medical Equipment , Ltd.

FDA 510(k) clearance K003251 for BLEASE FRONTLINE PLUS RANGE, ANESTHESIA MACHINES, MODEL 440, 560 AND 690, Substantially Equivalent on 2001-05-23. Applicant: Blease Medical Equipment , Ltd.. Device class: 2.

Clearance details

Applicant
Blease Medical Equipment , Ltd.
Product code
Code BSZ
Device class
Class 2
Regulation
21 CFR 868.5160
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Appollo Beach, FL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code BSZ

view all

More clearances from Blease Medical Equipment , Ltd.

view all

Adverse events under product code BSZ

product code BSZ
Death
23
Injury
298
Malfunction
32,987
Total
33,308

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 →

Recalls naming K003251

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K003251.

Data sourced from openFDA. This site is unofficial and independent of the FDA.