FDA PMA FDA Unclassified Approved 🇺🇸 United States

Lens, Contact (Polymethylmethacrylate)

PMA: P820063 · Supplement: S016 · Decision Jun 24, 1986
Classifications
1
FEI Numbers
9
Registration Numbers
9

Basic Information

Device Name
Lens, Contact (Polymethylmethacrylate)
Trade Name
PARAPERM O2 CONTACT LENS
PMA Number
P820063
Supplement Number
S016
Device Class
FDA Unclassified
Product Code
HPX
Generic Name
Lens, contact (polymethylmethacrylate)
Medical Specialty
Unknown
Advisory Committee
Ophthalmic
Decision
Approved
Decision Code
APPR
Decision Date
June 24, 1986
Date Received
June 9, 1986
Supplement Type
Normal 180 Day Track
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Classifications

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

Product Code Device Name
HPX Lens, Contact (Polymethylmethacrylate)