Cleared Traditional

K841793 - COOPER LASERSONICS ND:YAG LASER 8000 (FDA 510(k) Clearance)

K841793 · Cooper Lasersonics, Inc. · Cardiovascular device
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Jun 1984
Decision
38d
Days
-
Risk

K841793 is an FDA 510(k) clearance for the COOPER LASERSONICS ND:YAG LASER 8000.

Submitted by Cooper Lasersonics, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 7, 1984 after a review of 38 days - a notably fast clearance cycle.

This device falls under the Cardiovascular 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 Cooper Lasersonics, Inc. devices

Submission Details

510(k) Number K841793 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 30, 1984
Decision Date June 07, 1984
Days to Decision 38 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
87d faster than avg
Panel avg: 125d · This submission: 38d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -