KEELER MULTILASE 3000— 510(k) K942180

Substantially Equivalent

Keeler Instruments, Inc.

FDA 510(k) clearance K942180 for KEELER MULTILASE 3000, Substantially Equivalent on 1994-11-22. Applicant: Keeler Instruments, Inc..

Clearance details

Applicant: Keeler Instruments, Inc.
Product code: Code HQF
Advisory panel: Ophthalmic
Date received: 1994-05-04
Decision date: 1994-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Broomall, PA, US

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Adverse events under product code HQF

product code HQF

Injury: 166
Other: 1
Total: 167

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.