DeviceClearance

OPAQUE HERRICK LACRIMAL PLUG, 0.3MM,0.5MM,0.7MM, MODELS HLP3-OPB,HLP50OPB,HLP7-OPB— 510(k) K021831

Substantially Equivalent

Lacrimedics, Inc.

FDA 510(k) clearance K021831 for OPAQUE HERRICK LACRIMAL PLUG, 0.3MM,0.5MM,0.7MM, MODELS HLP3-OPB,HLP50OPB,HLP7-OPB, Substantially Equivalent on 2002-07-01. Applicant: Lacrimedics, Inc.. Device class: Unclassified.

Clearance details

Applicant
Lacrimedics, Inc.
Product code
Code LZU
Device class
Unclassified
Advisory panel
Unknown
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Eastsound, WA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code LZU

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More clearances from Lacrimedics, Inc.

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Adverse events under product code LZU

product code LZU
Other
2
Total
2

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 K021831

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 K021831.

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