Atlas FDA

PERMALID PAK

FDA 510(k) clearance K842781 · decided 1985-08-01

Clearance details

K-number
K842781
Device name
PERMALID PAK
Applicant
CooperVision, Inc.
Decision
Unknown
Date received
1984-07-16
Decision date
1985-08-01
Days to decision
381 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Southampton, GB
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch CooperVision

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

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