Cleared Traditional

LASERMED OCULASE ARGON LASER (K828583) - FDA 510(k) Clearance

K828583 · Lasermed Corp. · Radiology device
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Jan 1983
Decision
52d
Days
-
Risk

K828583 is an FDA 510(k) clearance for the LASERMED OCULASE ARGON LASER.

Submitted by Lasermed Corp. (Costa Mesa, US). The FDA issued a Cleared decision on January 14, 1983 after a review of 52 days - a notably fast clearance cycle.

This device falls under the Radiology 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: 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 Lasermed Corp. devices

Submission Details

510(k) Number K828583 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 23, 1982
Decision Date January 14, 1983
Days to Decision 52 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
55d faster than avg
Panel avg: 107d · This submission: 52d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -