Cleared Traditional

AGL400 ARGON LASER SYSTEM-KRL500 KRYPTON (K843345) - FDA 510(k) Clearance

K843345 · Mira, Inc. · Ophthalmic device
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Nov 1984
Decision
71d
Days
-
Risk

K843345 is an FDA 510(k) clearance for the AGL400 ARGON LASER SYSTEM-KRL500 KRYPTON.

Submitted by Mira, Inc. (Waltham, US). The FDA issued a Cleared decision on November 6, 1984 after a review of 71 days - a notably fast clearance cycle.

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: 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 Mira, Inc. devices

Submission Details

510(k) Number K843345 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 27, 1984
Decision Date November 06, 1984
Days to Decision 71 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
39d faster than avg
Panel avg: 110d · This submission: 71d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -