FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DOCUMENTING LASER SLIT LAMP, DP 2010

K Number: K012873 · Decision Nov 19, 2001
Classifications
1
FEI Numbers
54
Registration Numbers
55
Same Product Code
107
Applicant Total
92
Review Days
84

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DOCUMENTING LASER SLIT LAMP, DP 2010
K Number
K012873
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1850
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bausch & Lomb, Inc.
Date Received
August 27, 2001
Decision Date
November 19, 2001
Product Code
HJO
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
HJO Biomicroscope, Slit-Lamp, Ac-Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HJO), ordered by most recent decision date.

View all

Other Clearances by Bausch & Lomb, Inc.

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. →