FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

FLUROPERM 60-OK, PARAGON HDS-OK

K Number: K000224 · Decision Apr 17, 2000
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
5
Applicant Total
15
Review Days
84

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Basic Information

Device Name
FLUROPERM 60-OK, PARAGON HDS-OK
K Number
K000224
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5916
Medical Specialty
Ophthalmic
Decision
Unknown
Statement or Summary
Summary
Applicant
Paragon Vision Sciences
Date Received
January 24, 2000
Decision Date
April 17, 2000
Product Code
MUW
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
MUW Lens, Contact (Orthokeratology)

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Other Clearances by Paragon Vision Sciences

K Number Device Name
K180172 FluoroPerm 30 & Paragon Thin (paflufocon C) RGP contact lenses with Tangible Hydra-PEG; FluoroPerm 60 & Paragon HDS (paflufocon B) RGP contact lenses with Tangible Hydra-PEG; FluoroPerm 92 (paflufocon A) RGP contact lenses with Tangible Hydra-PEG; FluoroPerm 151 & Paragon HDS 100 (paflufocon D) RGP contact lenses with Tangible Hydra-PEG
K120996 FLUOROPERM 30 PARAGON HDS FLUOROPERM 60 PARAGON HDS 100 FLUOROPERM 92 FLUOROPERM 151 PARAGON THIN
K082799 HDS HI 1.54
K070637 FLUOROPERM 92, 60, 30 AND 151 AND PARAGON HDS, HDS 100 AND THIN RIGID GAS PERMEABLE CONTACT LENSES
K052983 FLUOROPERM 151 (PAFLUFOCON D) AND PARAGON HDS 100 (PAFLUFOCON D) RIGID GAS PERMEABLE CONTACT LENSES
K013310 PVS BASIC 2; EPIC 2
K010109 FLUOROPERM 151-OK, PARAGON HDS 100-OK
K002845 PAFLUFOCON C AND E DAILY CONTACT LENS
K993586 SPORTSIGHT GP
K993486 PARAGON LENS CARRIER
Search all 15 clearances from Paragon Vision Sciences →