FDA PMA FDA Class 3 Approved 🇺🇸 United States

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

PMA: P850001 · Supplement: S002 · Decision Sep 18, 1985
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
HORIZON(TM) YAG LASER MODEL 2000
PMA Number
P850001
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
September 18, 1985
Date Received
March 25, 1985
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