Cleared Traditional

K883719 - INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM

K883719 is an FDA 510(k) clearance for INTERCONN. OF OPHTHALAS & NANOLAS LASER..., manufactured by Biophysic Medical, Inc.. The device is a Class 2 Ophthalmic device with product code LQJ cleared through the Traditional 510(k) pathway after a 48-day FDA review.

K883719 · Biophysic Medical, Inc. · Ophthalmic device
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Oct 1988
Decision
48d
Days
Class 2
Risk

K883719 is an FDA 510(k) clearance for the INTERCONN. OF OPHTHALAS & NANOLAS LASER SYSTEM. Classified as Lens, Surgical, Laser, Accesssory, Ophthalmic Laser (product code LQJ), Class II - Special Controls.

Submitted by Biophysic Medical, Inc. (Pleasant Hill, US). The FDA issued a Cleared decision on October 18, 1988 after a review of 48 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4390 - the FDA ophthalmic device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Biophysic Medical, Inc. devices

FDA 510(k) Submission Details - K883719

510(k) Number K883719 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 31, 1988
Decision Date October 18, 1988
Days to Decision 48 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
62d faster than avg
Panel avg: 110d · This submission: 48d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LQJ Device Classification - Class 2, Special Controls

Product Code LQJ Lens, Surgical, Laser, Accesssory, Ophthalmic Laser
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 886.4390
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Ophthalmic devices follow this clearance model.

Regulatory Peers - LQJ Lens, Surgical, Laser, Accesssory, Ophthalmic Laser

All 8
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