DeviceClearance

ORIGIN BLUNT TIP SURGICAL TROCAR— 510(k) K924011

Substantially Equivalent

Origin Medsystems, Inc.

FDA 510(k) clearance K924011 for ORIGIN BLUNT TIP SURGICAL TROCAR, Substantially Equivalent on 1993-07-09. Applicant: Origin Medsystems, Inc.. Device class: 2.

Clearance details

Applicant
Origin Medsystems, Inc.
Product code
Product code GCJ
Device class
Class 2
Regulation
21 CFR 876.1500
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Menlo Park, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code GCJ

product code GCJ
Death
39
Injury
1,638
Malfunction
28,216
Other
11
Total
29,904

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 K924011

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 K924011.

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