FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR

K Number: K862519 · Decision Jul 23, 1986
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
8
Applicant Total
92
Review Days
22

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Basic Information

Device Name
BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR
K Number
K862519
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.1680
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Bausch & Lomb, Inc.
Date Received
July 1, 1986
Decision Date
July 23, 1986
Product Code
HOS
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HOS Projector, Ophthalmic

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K Number Device Name
K192005 Bausch + Lomb PreVue Inserter for enVista Preloaded
K173480 Crystalsert Lens Delivery System
K151102 Bausch + Lomb Injector System
K131208 BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS, BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS FOR PRESBYOPIA,
K122575 BAUSCH & LOMB PUREVISION (BALAFILCON A) VISIBILITY TINTED CONTACT LENS, BAUSCH & LOMB PUREVISION TORIC (BALAFILCON A) VI
K113852 BAUSCH & LOMB IOL INJECTOR
K112909 OCD04 3% HYDROGEN PEROXIDE CLEANING AND DISINFECTING SOULTION
K111877 EZS05 CLEANING AND DISINFECTING SOLUTION, BAUSCH + LOMB EZS05 CLEANING AND DISINFECTING SOLUTION
K112192 NATURELLE DAILY DISPOSABLE (HILAFILCON B) COSMETICALLY TINTED CONTACT LENS
K101325 STELLARIS PC VISION ENHANCEMENT SYSTEM
Search all 92 clearances from Bausch & Lomb, Inc. →