Cleared Traditional

K800697 - SUNHOUSE UVB ULTRAVIOLET LIGHT TANNING (FDA 510(k) Clearance)

Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1980
Decision
35d
Days
-
Risk

K800697 is an FDA 510(k) clearance for the SUNHOUSE UVB ULTRAVIOLET LIGHT TANNING.

Submitted by Progressive Productions , Ltd. (Mchenry, US). The FDA issued a Cleared decision on May 2, 1980 after a review of 35 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 Progressive Productions , Ltd. devices

Submission Details

510(k) Number K800697 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 28, 1980
Decision Date May 02, 1980
Days to Decision 35 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
72d faster than avg
Panel avg: 107d · This submission: 35d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -