SAFESET RESERVOIR— 510(k) K932188

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K932188 for SAFESET RESERVOIR, Substantially Equivalent on 1993-10-25. Applicant: Abbott Laboratories. Device class: 2.

Clearance details

Applicant
Abbott Laboratories
Product code
Code KRA
Device class
Class 2
Regulation
21 CFR 870.1210
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Abbott Park, IL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code KRA

view all

More clearances from Abbott Laboratories

view all

Adverse events under product code KRA

product code KRA
Death
234
Injury
1,029
Malfunction
3,012
Other
2
Total
4,277

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 K932188

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 K932188.

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