PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS— 510(k) K864003

Substantially Equivalent

Allergan, Inc.

FDA 510(k) clearance K864003 for PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS, Substantially Equivalent on 1986-10-31. Applicant: Allergan, Inc..

Clearance details

Applicant: Allergan, Inc.
Product code: Code HNR
Advisory panel: Ophthalmic
Date received: 1986-10-14
Decision date: 1986-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ana, CA, US

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Adverse events under product code HNR

product code HNR

Malfunction: 497
Other: 1
Total: 498

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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