Cleared Traditional

K827379 - X-RAY CASSETTE (FDA 510(k) Clearance)

K827379 · Synchroplan Corp. · Radiology device
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May 1982
Decision
30d
Days
-
Risk

K827379 is an FDA 510(k) clearance for the X-RAY CASSETTE.

Submitted by Synchroplan Corp. (New York, US). The FDA issued a Cleared decision on May 19, 1982 after a review of 30 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 Synchroplan Corp. devices

Submission Details

510(k) Number K827379 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 19, 1982
Decision Date May 19, 1982
Days to Decision 30 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
77d faster than avg
Panel avg: 107d · This submission: 30d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -