Cleared Traditional

K827087 - P1808 MOBILE C-ARM IMAGE INTENSIFIER (FDA 510(k) Clearance)

K827087 · Precise Optics · Radiology device
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Mar 1982
Decision
41d
Days
-
Risk

K827087 is an FDA 510(k) clearance for the P1808 MOBILE C-ARM IMAGE INTENSIFIER.

Submitted by Precise Optics (Bay Shore, US). The FDA issued a Cleared decision on March 4, 1982 after a review of 41 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 Precise Optics devices

Submission Details

510(k) Number K827087 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 22, 1982
Decision Date March 04, 1982
Days to Decision 41 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
66d faster than avg
Panel avg: 107d · This submission: 41d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -