Atlas FDA

R PAK

FDA 510(k) clearance K851203 · decided 1985-07-23

Clearance details

K-number
K851203
Device name
R PAK
Applicant
CooperVision, Inc.
Decision
Substantially Equivalent
Date received
1985-03-26
Decision date
1985-07-23
Days to decision
119 days
Clearance type
Traditional
Product code
LFL
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Irvine, CA, US
Third-party review
No
Expedited review
No

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Devices cleared under the same product code - the starting set for predicate research.

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear (P180035/S033)CooperVision, Inc.2025-12-23
MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear (P180035/S032)CooperVision, Inc.2025-12-17
Biofinity XR Toric and Biofinity Toric Multifocal (Comfilcon A) Soft (Hydrophilic) Contact Lenses for Extended Wear (P080011/S193)CooperVision, Inc.2025-12-11
Sofmed® breathables™ XW NEXT (P080011/S191)CooperVision, Inc.2025-12-05
MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear (P180035/S031)CooperVision, Inc.2025-10-28
Biofinity Toric Multifocal and Biofinity XR Toric (comfilcon A) Soft (Hydrophilic) Contact Lenses for Extended Wear (P080011/S192)CooperVision, Inc.2025-09-22
up&up Monthly Performance + (P080011/S184)CooperVision, Inc.2025-08-20
iWear oxygen presbyopia (P080011/S186)CooperVision, Inc.2025-08-20