DeviceClearance

AURORA LED SERIES SURGICAL LIGHTS— 510(k) K071698

Substantially Equivalent

Skytron, Div. the Kmw Group, Inc.

FDA 510(k) clearance K071698 for AURORA LED SERIES SURGICAL LIGHTS, Substantially Equivalent on 2007-07-06. Applicant: Skytron, Div. the Kmw Group, Inc.. Device class: 2.

Clearance details

Applicant
Skytron, Div. the Kmw Group, Inc.
Product code
Code FSY
Device class
Class 2
Regulation
21 CFR 878.4580
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Grand Rapids, MI, US
Download summary PDFView on FDA.gov ↗

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More clearances from Skytron, Div. the Kmw Group, Inc.

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Adverse events under product code FSY

product code FSY
Malfunction
2,759
Other
1
Total
2,760

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 K071698

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 K071698.

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