FDA PMA FDA Class 3 Approved 🇺🇸 United States

Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

PMA: P840047 · Supplement: S002 · Decision Jan 9, 1987
Classifications
1
FEI Numbers
0
Registration Numbers
0

Basic Information

Device Name
Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary
Trade Name
CILCO ND:YAG LASER
PMA Number
P840047
Supplement Number
S002
Device Class
FDA Class 3
Product Code
LOI
Generic Name
Laser, neodymium:Yag, ophthalmic for uses other than posterior capsulotomy & cutting pupillary
Medical Specialty
Unknown
Advisory Committee
Ophthalmic
Decision
Approved
Decision Code
APPR
Decision Date
January 9, 1987
Date Received
November 28, 1986
Supplement Type
Normal 180 Day Track
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LOI Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary