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

ALCON MULTI-PURPOSE DISINFECTING SOLUTION

K Number: K050729 · Decision Sep 14, 2005
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
119
Applicant Total
16
Review Days
177

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Basic Information

Device Name
ALCON MULTI-PURPOSE DISINFECTING SOLUTION
K Number
K050729
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5928
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alcon Research, Ltd.
Date Received
March 21, 2005
Decision Date
September 14, 2005
Product Code
LPN
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
LPN Accessories, Soft Lens Products

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Other Clearances by Alcon Research, Ltd.

K Number Device Name
K161794 CENTURION Vision System (Active SentryTM)
K170520 HyperVit Vitrectomy Probe, 23 GA, HyperVit Vitrectomy Probe, 25+, HyperVit Vitrectomy Probe, 27+
K141065 CONSTELLATION VISION SYSTEM
K121031 WAVELIGHT FS200 PATIENT INTERFACE 1505
K112977 MONARCH III IOL DELIVERY SYSTEM, MONARCH III C CARTRIDGE, MONARCH III HANDPIECE (H4)
K110951 27+ ULTRAVIT PROBE, 27+ FLEX-TIP LASER PROBE, 27+ ENDOILLUMINATOR PROBE, 27+ VALVED ENTRY SYSTEM, 27+ INFUSION CANNULA
K110166 CLEARCUT S SAFETY KNIFE
K102860 ALCON MULTI-PIRPOSE DISINFECTING SOLUTION
K101006 WAVELIGHT FS200 LASER SYSTEM MODEL: FS200
K093305 ENHANCED ULTRA VIT PROBE
Search all 16 clearances from Alcon Research, Ltd. →