Single Use Injector NM600/610— 510(k) K153625

Substantially Equivalent

Olympus Medical Systems Corp.

FDA 510(k) clearance K153625 for Single Use Injector NM600/610, Substantially Equivalent on 2016-02-12. Applicant: Olympus Medical Systems Corp.. Device class: 2.

Clearance details

Applicant
Olympus Medical Systems Corp.
Product code
Code FBK
Device class
Class 2
Regulation
21 CFR 876.1500
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Hachioji-Shi, JP
Download summary PDFView on FDA.gov ↗

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Adverse events under product code FBK

product code FBK
Other
1
Total
1

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 K153625

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 K153625.

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