PRE-MOISTENED CLEANSING PAD— 510(k) K890514
Substantially EquivalentBausch & Lomb, Inc.
FDA 510(k) clearance K890514 for PRE-MOISTENED CLEANSING PAD, Substantially Equivalent on 1989-04-10. Applicant: Bausch & Lomb, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Bausch & Lomb, Inc.
- Product code
- Code LKB
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rochester, NY, US
Recent devices under product code LKB
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- K151102 — Bausch + Lomb Injector System
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- K122575 — BAUSCH & LOMB PUREVISION (BALAFILCON A) VISIBILITY TINTED CONTACT LENS, BAUSCH & LOMB PUREVISION TORIC (BALAFILCON A) VI
Adverse events under product code LKB
product code LKB- 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 →
Data sourced from openFDA. This site is unofficial and independent of the FDA.