Cleared Traditional

K853807 - ALL-IN-ONE HARD CONTACT LENS SOLUTION

K853807 · Maurry Biological Co. · Ophthalmic device
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Dec 1985
Decision
96d
Days
-
Risk

K853807 is an FDA 510(k) clearance for the ALL-IN-ONE HARD CONTACT LENS SOLUTION. Classified as Lens, Contact (polymethylmethacrylate) (product code HPX).

Submitted by Maurry Biological Co. (Los Angeles, US). The FDA issued a Cleared decision on December 16, 1985 after a review of 96 days - within the typical 510(k) review window.

This device falls under the Ophthalmic FDA review panel. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Ophthalmic review framework, consistent with the majority of Class II 510(k) submissions.

View all Maurry Biological Co. devices

FDA 510(k) Submission Details - K853807

510(k) Number K853807 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 11, 1985
Decision Date December 16, 1985
Days to Decision 96 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
14d faster than avg
Panel avg: 110d · This submission: 96d
Pathway characteristics
Predicate-based equivalence.

HPX Device Classification - Class 0,

Product Code HPX Lens, Contact (polymethylmethacrylate)
Device Class -

Regulatory Peers - HPX Lens, Contact (polymethylmethacrylate)

All 20
Devices cleared under the same product code (HPX) and FDA review panel - the closest regulatory comparables to K853807.
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BAUSCH & LOMB LENS CARRYING CASE
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SIGHT SAVER ALL PURPOSE LENS CARRYING CASE
K852384 · Bausch & Lomb, Inc. · Jul 1985
SENSITIVE EYES
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K830740 · CooperVision, Inc. · Jun 1983