FDA PMA FDA Unclassified Approved 🇺🇸 United States

Lens, Contact (Polymethylmethacrylate)

PMA: P820063 · Supplement: S037 · Decision Nov 28, 1988
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
S037
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
November 28, 1988
Date Received
November 9, 1988
Supplement Type
THIRTY 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)