ALCON SURGICAL PROCEDURE PACKS— 510(k) K880961

Substantially Equivalent

Alcon Laboratories

FDA 510(k) clearance K880961 for ALCON SURGICAL PROCEDURE PACKS, Substantially Equivalent on 1988-04-29. Applicant: Alcon Laboratories. Device class: 2.

Clearance details

Applicant
Alcon Laboratories
Product code
Code LRO
Device class
Class 2
Regulation
21 CFR 878.4370
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Fort Worth, TX, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code LRO

product code LRO
Injury
975
Malfunction
14,038
Other
2
Total
15,015

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 K880961

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 K880961.

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